Mutation of a Nopp140 gene dao-5 alters rDNA transcription and increases germ cell apoptosis in C. elegans

Abstract

Human diseases of impaired ribosome biogenesis resulting from disruption of rRNA biosynthesis or loss of ribosomal components are collectively described as 'ribosomopathies'. Treacher Collins syndrome (TCS), a representative human ribosomopathy with craniofacial abnormalities, is attributed to mutations in the tcof1 gene that has a homologous gene called nopp140. Previous studies demonstrated that the dao-5 (dauer and aged animal overexpression gene 5) of Caenorhabditis elegans is a member of nopp140 gene family and plays a role in nucleogenesis in the early embryo. Here, we established a C. elegans model for studying Nopp140-associated ribosomopathy. A null dao-5 mutant ok542 with a semi-infertile phenotype showed a delay in gonadogenesis, as well as a higher incidence of germline apoptosis. These phenotypes in dao-5(ok542) are likely resulted from inefficient rDNA transcription that was observed by run-on analyses and chromatin immunoprecipitation (ChIP) assays measuring the RNA Pol I occupancy on the rDNA promoter. ChIP assays further showed that the modifications of acetylated histone 4 (H4Ac) and dimethylation at the lysine 9 of histone 3 (H3K9me2) around the rDNA promoter were altered in dao-5 mutants compared with the N2 wild type. In addition, activated CEP-1 (a C. elegans p53 homolog) activity was also linked to the loss of DAO-5 in terms of the transcriptional upregulation of two CEP-1 downstream effectors, EGL-1 and CED-13. We propose that the dao-5 mutant of C. elegans can be a valuable model for studying human Nopp140-associated ribosomopathy at the cellular and molecular levels.

OPEN

Citation: Cell Death and Disease (2014) 5, e1158; doi:10.1038/cddis.2014.114

& 2014 Macmillan Publishers Limited All rights reserved 2041-4889/14 http://www.nature.com/cddis

Web End =www.nature.com/cddis

C-C Lee1,4, Y-T Tsai2,3,4,5, C-W Kao2, L-W Lee2, H-J Lai2, T-H Ma2,3, Y-S Chang2,3, N-H Yeh1 and SJ Lo*,1,2

Human diseases of impaired ribosome biogenesis resulting from disruption of rRNA biosynthesis or loss of ribosomal components are collectively described as ribosomopathies. Treacher Collins syndrome (TCS), a representative human ribosomopathy with craniofacial abnormalities, is attributed to mutations in the tcof1 gene that has a homologous gene called nopp140. Previous studies demonstrated that the dao-5 (dauer and aged animal overexpression gene 5) of Caenorhabditis elegans is a member of nopp140 gene family and plays a role in nucleogenesis in the early embryo. Here, we established aC. elegans model for studying Nopp140-associated ribosomopathy. A null dao-5 mutant ok542 with a semi-infertile phenotype showed a delay in gonadogenesis, as well as a higher incidence of germline apoptosis. These phenotypes in dao-5(ok542) are likely resulted from inefcient rDNA transcription that was observed by run-on analyses and chromatin immunoprecipitation (ChIP) assays measuring the RNA Pol I occupancy on the rDNA promoter. ChIP assays further showed that the modications of acetylated histone 4 (H4Ac) and dimethylation at the lysine 9 of histone 3 (H3K9me2) around the rDNA promoter were altered in dao-5 mutants compared with the N2 wild type. In addition, activated CEP-1 (a C. elegans p53 homolog) activity was also linked to the loss of DAO-5 in terms of the transcriptional upregulation of two CEP-1 downstream effectors, EGL-1 and CED-13. We propose that the dao-5 mutant of C. elegans can be a valuable model for studying human Nopp140-associated ribosomopathy at the cellular and molecular levels.

Cell Death and Disease (2014) 5, e1158; doi:http://dx.doi.org/10.1038/cddis.2014.114

Web End =10.1038/cddis.2014.114 ; published online 10 April 2014

Subject Category: Experimental Medicine

Reliable ribosome biogenesis is essential to cell growth and maintenance. Impairments in ribosome biogenesis that are caused by genetic mutations of nucleolus-associated proteins or ribosomal proteins have been described as nucleolar stress or ribosomal stress (for review, see Boulon et al.1 and references therein). Recently, various human genetic diseases such as DiamondBlackfan anemia (DBA),SchwachmanDiamond syndrome (SDS), X-linked dyskeratosis congenita (DKC), cartilage hair hypoplasia (CHH), andTreacher Collins syndrome (TCS) have been associated with impaired ribosome biogenesis and functions, and are jointly referred to as ribosomopathies (for review, see Narla andEbert2 and references therein). Although each disease results from defects in various aspects in ribosome biogenesis, for example, the mutations found in ribosomal protein genes (DBA and SDS) or the genes encoding factors associated with ribosomal DNA (rDNA) transcription (TCS) and ribosomal RNA (rRNA) processing (DKC), respectively, the resultant diseases display distinct clinical symptoms, most of which involve bone marrow failure, skeletal, and/or craniofacial defects.3

Keywords: nucleolus; ribosomopathy; Nopp140; rDNA; evolution

Abbreviations: ChIP, chromatin immunoprecipitation; Nopp140, nucleolar phosphorylated protein of 140 kD; TCS, Treacher Collins syndrome; snoRNP, small nucleolar ribonucleoprotein

Mutation of a Nopp140 gene dao-5 alters rDNA transcription and increases germ cell apoptosis in C. elegans

Notably, the etiological mutations of human TCS are heterogeneous. Autosomal mutations in the tcof1 gene that encodes a nucleolar protein known as Treacle provide the major link to TCS pathogenesis,4 whereas a minority of TCS individuals with intact Treacle (8%) have recently been identied to harbor mutated POLR1D or POLR1C, the common subunits of RNA polymerase I and III.5 Treacle has also been shown to play an important role in rDNA transcription6 and is implicated in 2-O-methylation of 18S rRNA for maturation.7 A homolog of Treacle, Nopp140 (nucleolar phosphorylated protein of 140 kD), which has as yet no human disease associated with it, could potentially be involved in ribosomopathogenesis.

Nopp140 is a highly phosphorylated protein whose tripartite organization is highly conserved and similar toTreacle (Figure 1a). Both nucleolar proteins can bind to the rDNA chromatin and participate in rDNA transcription via theirC-terminal domains, respectively.8,9 Nopp140 was rst demonstrated to be a chaperon for shuttling between the nucleolus and cytoplasm in rat liver cells.10 Nopp140 has also

1Institute of Microbiology and Immunology, National Yang-Ming University, Taipei 112, Taiwan; 2Department and Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan and 3Molecular Medicine Research Center, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan *Corresponding author: SJ Lo, Department of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan. Tel: [phone], ext. 3295; Fax: [phone]; E-mail: mailto:[email protected]

Web End [email protected]

4These authors contributed equally to this work.

5Current address: Institute of Molecular Medicine and Genetics, Georgia Regents University, Augusta, Georgia, USA

Received 18.4.13; revised 17.2.14; accepted 20.2.14; Edited by Y Shi

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Figure 1 Protein features among human Treacle, Nopp140, and C. elegans DAO-5 and amino acid alignment of the C-termini. (a) Scheme of the tripartite features, which possess an N-terminal domain, a central acid-basic domain, and a C-terminal domain of human and C. elegans Nopp140, and human Treacle are shown, respectively. The explanation of each colored domain is indicated below. The number at the end of schemes indicates the total amino acid residues of each protein. (b) The C-terminal domain of Nopp140s is highly conserved across metazoans. The residues in yellow are identically conserved and residues in blue are highly conserved whereas the moderately conserved residues are shown in green. The highly conserved stretches of amino acid residues between C. elegans and humans are indicated with a line above the alignment. Hs, Homo sapiens; Rn, Rattus norvegicus; Mm, Mus musculus; Cf, Canis familiaris; Gg, Gallus gallus; Xl, Xenopus laevis; Xt, Xenopus tropicalis; Dm, Drosophila melanogaster; Ce, Caenorhabditis elegans; Cb, Caenorhabditis briggsae; Sc, Saccharomyces cerevisiae; Sp, Schizosaccharomyces pombe; Tb, Trypanosoma brucei

been reported to be an RNA pol II transcriptional regulator11

and a binding target of doxorubicin,12 an anticancer agent. Reports show that human Nopp140 (hNopp140) plays important roles in rRNA biosynthesis by interacting with the largest subunit of RNA polymerase I (Pol I) in HeLa cells.13 In

addition, hNopp140 can bind to the rDNA and a-satellite array and thus it has been proposed to function as a scaffold protein for maintaining the integrity of rDNA transcription and the nucleolar structure.9 According to functions linked to the identied Nopp140-associated proteins, including NAP57 (Nopp140 associating protein of 57 kD), NAP65, and p80-coilin, it has been suggested that Nopp140 might also play a role in rRNA processing as a small nucleolar ribonucleoprotein (snoRNP) chaperon (for review, see He and Dimario14

and Lo et al.15 and references therein). NAP57 (also known as dyskerin) is a component of box H/ACA snoRNPs that participates in pseudouridylation of pre-rRNA.16 Of note,

mutation of the NAP57 gene in humans leads to another important ribosomopathy disease, dyskeratosis congenita (see above). Altogether, Nopp140 is tightly associated with rRNA biosynthesis and might also be implicated in ribosomopathic etiology.

To gain insights into Nopp140-dependent ribosomopathy, an animal model has been developed. Previously, a Drosophila Nopp140 model showed that ies with depletions of Nopp140 exhibited minute-like phenotypes, including malformed wings, legs, and tergites that are phenotypes highly associated with ribosomal protein insufciency.17

Because of the tractability of the nematode Caenorhabditis elegans, including shorter life cycle, transparent body, and easy handling,18 we used C. elegans as an alternative animal model for investigating Nopp140 biology. We have found that a mutant of dao-5, a C. elegans Nopp140 homolog, exhibits severe gonadal defects because of impaired rRNA synthesis.

Results

DAO-5 is a member of the Nopp140 family with a highly conserved C-terminal domain. To search for a Nopp140 homolog in the C. elegans, the full length of 699 residues of hNopp140 was used to BLAST Wormbase (http://www.wormbase.org

Web End =www.wormbase. http://www.wormbase.org

Web End =org ). The highest scored hit was ORF C25A1.10 that has been annotated as dao-5 for dauer and aged animal overexpression.19 It encodes a protein with 971 amino acid residues that contains a high percentage of four amino acids, Lys, Ser, Ala, and Asp, comprising 460% of the total residues. Amino acid sequence analysis revealed that C25A1.10 consists of three domains similar to hNopp140, but with 15 extra repeats within the central acid-basic domain (Figure 1a). The consensus sequence of the repeat in C25A1.10 is DSSSDSSDDEAPAKKTPAKAAPKPASKKA, similar to that of hNopp140: DSSSEEEKKPPTKAVVSKATTKPPAKKAAE. As the C-termini of Nopp140s from yeasts to mammals are evolutionarily conserved, which may reect their functional importance,9,20 the C-termini of Nopp140s and DAO-5 were aligned to highlight the sequence conservation (Figure 1b). The sequence alignment revealed that DAO-5 shares a higher percentage of identity to mammals than to unicellular organisms. Specically, three continuous stretches (SSPFRRV, FRHEKTKKKRGSY, and NSIKF) at the same positions are identical to hNopp140 (Figure 1b).

DAO-5 is a nucleolar protein expressed in various tissues. Previously, a panel of monoclonal antibodies was generated by Hadwiger et al.21 as a toolkit for studyingC. elegans, and one of them, the monoclonal antibody 5E9, has been demonstrated to recognize DAO-5 as a nucleolar marker. Later, Korcekova et al.22 used the 5E9 monoclonal

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antibody to show the importance of DAO-5 during nucleogenesis in C. elegans embryo. To further study the DAO-5 expression pattern in a whole worm, we generated a transgenic worm carrying an extrachromosomal array of Pdao-5::dao-5::gfp that expressed a fusion protein of DAO-5 with green uorescence protein (DAO-5::GFP). The DAO-5::GFP appeared in oval- to round-shaped dots, a typical appearance of nucleoli, in various tissues including nerve ring, intestine, and hypodermis (Figure 2a). Because of the germline silencing effect,23 the transgenic worms did not express DAO-5::GFP in germ cells. We dissected gonad and intestine of transgenic animals and stained with an anti-brillarin (a nucleolus marker24) antibody. We found that the ectopically expressed DAO-5::GFP was clearly colocalized with brillarin in the nucleoli of the somatic gonad (sheath cells) and intestinal cells (Figure 2b), indicating that the DAO-5 is indeed localized to nucleoli. Consistently, another transgenic worm carrying an inserted transgene of Ppie-1::ORFdao-5::

gfp-30UTRdao-5 (designated as cguIs13), whose germline expressed DAO-5::GFP, also revealed its nucleolar localization (Supplementary Figure S1) as previously shown.21

DAO-5 forms a complex with RNA Pol I. To further test whether DAO-5 is also an RNA Pol I binding partner similar to hNopp140,13 cell lysates from N2 worms were immuno-precipitated with anti-Pol I antibodies or a control antibody followed by western blot analyses with the anti-DAO-5 antibody 5E9. Results showed that the endogenous DAO-5 could be specically coprecipitated with RNA Pol I (Figure 2c). Taken together, we revealed that DAO-5, which is expressed in various tissues, not only predominately localizes at nucleoli but also appears similar in character to hNopp140 by forming complexes with RNA Pol I.13

The association of DAO-5 with rDNA. Next, we examined whether DAO-5 also interacts with rDNA in a manner similar to hNopp140.9 C. elegans rDNA is B7 kb, and the rDNA cluster is located at the right arm of chromosome I (Figure 2d).25,26 We performed chromatin immunoprecipitation (ChIP) assays to examine the endogenous DAO-5 occupancy on rDNA clusters. DAO-5 showed specic binding to the rDNA promoter region (Figure 2d) as well as the regions within the rRNA gene body (26S rRNA) and rDNA terminator. Notably, the lysate from a deletion mutant of dao-5(ok542) obtained from the Caenorhabditis Genetics Center, which possesses a 1.7-kb truncation (Supplementary Figure S2), exhibits little or no enrichment compared with the wild-type counterpart, indicating that the truncated gene product cannot be recognized by the 5E9 antibody. On the other hand, compared with the signicant binding to the rDNA region, the DAO-5 occupancies on the promoter regions of brillarin (a Pol II gene) or 5S rRNA (a Pol III gene) were relatively low and insignicant between N2 and dao-5(ok542) animals (Supplementary Figure S3), suggesting that DAO-5 specically interacts with Pol I-dedicated rRNA genes. Consistent with the results observed by Korcekova et al.,22 we further demonstrated that the association of DAO-5 with rDNA and brillarin not only occurs in the early embryo, but also appears to be conserved throughout the organism.

Mutants of dao-5 display gonadal defects and produce smaller broods. To better understand the role that DAO-5 plays at the organismal level, we carried out more phenotypic analyses. Although the dao-5(ok542) homozygote animal is still viable, the fertility is signicantly damaged (Figure 3a). In the wild-type C. elegans hermaphrodite, the germline undergoes a prominent amplication to give rise to mature oocytes.27 Although the gonadal development of dao-5(ok542) appeared normal until the fourth larval stage (L4) (Figures 3b and c), adult worms showed delayed oogenesis and consequently underdeveloped gonads (Figures 3b and c). Importantly, the phenotypes were also observed in wild-type worms with dao-5(RNAi) knockdown (data not shown), and the semisterility phenotype of dao-5(ok542) could be rescued in dao-5(ok542); cguIs13 worms (Figures 3a and c), indicating that the fusion protein of DAO-5::GFP is functional and the germline expression of DAO-5 is sufcient for normal germline development, in particular oogenesis, the process where germ cells give rise to mature oocytes. Besides, no notable defects were found in the spermatheca in the dao-5(ok542) hermaphrodites (data not shown), and this supports our conclusion that the poor fertility of dao-5 mutants is attributed to the oogenic defect.

The dao-5 mutant displays a higher rate of germline apoptosis. As oogenesis was compromised in dao-5(ok542) mutants, we next examined whether one of the crucial landmarks in germline development, physiological apoptosis (also known as constitutive apoptosis),28 was also

affected. To monitor germ cell death, we applied a reporter transgene, bcIs39 [Plim-7::ced-1::gfp], to visualize the dying cells.29 In dao-5(ok542) background, there were signicantly increased CED-1::GFP-labeled cells in gonads as compared with those in bcIs39 animals (Figure 3d). Although there is no strict correlation between germ cell apoptosis culling and brood size control,30 such an increase in germ cell apoptosis also suggests that loss of DAO-5 affects gonadal development and oogenesis.

The rDNA transcription efcacy is reduced in dao-5(ok542) mutants. As DAO-5 serves as an RNA Pol I binding partner and binds to rDNA similar to its human counterpart (see above), we sought to learn whether the loss of DAO-5 would also compromise rDNA transcription, as observed in HeLa cells.9 We compared the in situ run-on activities between embryonic cell cultures from N2 and dao-5(ok542) animals. Based on a rationale that rDNA loci are the most actively transcribed genes in an eukaryotic cell,31 levels of the newly synthesized pre-rRNA are reected in the nucleolar uptake of Br-UTP after a brief pulse in cells. With a 5-min exposure of Br-UTP, there was a clear distinction in Br-UTP incorporating pattern between wild-type and dao-5(ok542) cells (Figure 4a, upper two panels), of which dao-5(ok542) showed lower intensity of Br-UTP signal in nucleoli. However, intensities of Br-UTP signals in a longer pulse (30 min) were similar (Figure 4a, lower two panels). To conrm whether the 30-min Br-UTP incorporation can validate the difference in the nascent rRNA level between wild-type and dao-5(ok542) cells, we performed a quantitative dot-blot assay of Br-UTP-containing RNA (see Materials

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Figure 2 DAO-5 is colocalized with brillarin and RNA polymerase I, and binds to rDNA. (a) A prole of DAO-5::GFP in a transgenic worm carrying Pdao-5::dao-5::gfp. The head of the worm is toward the right. The confocal uorescence image is shown in the upper panel and the superimposed image merged from the uorescence and bright eld channels is shown in the lower panel. The right panel is enlarged and turned 90-degree clock-wise from the rectangle indicated portion of worms at a low magnication. Arrowhead and arrow indicate the nucleoli in intestine cells and hypodermis cells, respectively. In, intestine; Ph, pharynx. Bar indicates 100 mm. (b) Ectopically expressed

DAO-5::GFP by an extrachromosomal array is localized in the nucleoli of somatic gonad and intestine and colocalized with brillarin, a common nucleolar marker. Arrowheads indicate sheath cells and bar represents 20 mm. (c) Immunoprecipitation by anti-Pol I antibody (lane 4, indicated by RPA194) or a control antibody (lane 3, indicated by IgG)

followed by western blot analysis probed by anti-DAO-5 antibody. Lanes 1 and 2 are total lysate input to show the presence of DAO-5 in N2 worms. Protein size markers are shown in kDa and the migration positions of DAO-5 are indicated with symbol of * at right. (d) Chromatin immunoprecipitation (ChIP) assay revealed that endogenous DAO-5 binds to the rDNA promoter region, gene body (26S rDNA), and terminator region. A scheme of rDNA and primers (with pairs of arrows) corresponding to the region of rDNA used for the ChIP assay are shown at top. Error bars represent S.D., n 3

and Methods). As a-amanitin, the inhibitor of RNA Pol II and III, was included in the transcription mix, the signal detected on the membrane could be regarded as generally the Pol I-mediated transcriptional output. Three independent experiments showed the results of 42 to 67% in the amount of Br-UTP-labeled RNA in dao-5(ok542) cells as compared with that of N2 cells. These results suggested that nascent rRNA was lower in the dao-5(ok542) mutant. Moreover, the binding of RNA Pol I on the rDNA promoter was also found to be 30% less in dao-5(ok542) worms (Figure 5a). Taken together, the Br-UTP incorporation results, and the Pol I occupancy on rDNA promoter, revealed that the rDNA transcription becomes inefcient in the absence of DAO-5, suggesting that DAO-5 plays a facilitating role for maintaining the

efciency of RNA Pol I-mediated rDNA transcription inC. elegans.

The ablation of DAO-5 reduces active rDNA chromatin states around the promoter. As one of the most pronounced cellular activities, rDNA transcription is heavily regulated, including its chromatin status.32 As DAO-5 readily binds the rDNA loci, we determined whether inefcient rDNA transcription in the absence of DAO-5 was the consequence of an altered chromatin state of rDNA. We conducted ChIP assays with three specic antibodies against various histone modication marks to detect the respective rDNA promoter binding abundance. First, the level of acetylated-histone H4 (H4ac), an active mark, was found to be signicantly

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Figure 3 The absence of DAO-5 results in compromised germline development. (a) The brood size counting of N2, dao-5(ok542), and the rescuing transgenic (cguIs13) animals. Data are meanS.D. N2 24713.06 (n 5); dao-5(ok542) 18.639.89 (n 8); dao-5(ok542); cguIs13 243.942.3 (n 11). Error bars represent the

S.D. (b) The dao-5(ok542) worms exhibit a delay in gonadogenesis. N2 and dao-5(ok542) animals were xed at the post-L4 stage at 12 h. Nuclei were highlighted with Hoechst 33342. The outlined scheme of the gonads is shown at right. MT, mitotic zone; TZ, transition zone; PC, pachytene; OO, oocytes; SP, spermetheca. (c) Time-course analysis showed a dao-5(ok542) hermaphrodite has a pronounced delay in germline development compared with wild-type N2 animals. The cguIs13 animal expresses a rescuing transgene that almost fully recovers the delayed pattern observed in the ok542 background. The average length of animals examined was as follows: for post-L4 0 h, N2 224.413.47 (n 9), dao-5(ok542) 202.821.96 (n 10), and dao-5(ok542); cguIs13 211.820.91 (n 4). For post-L4 12 h, N2 377.124.94 (n 11),

ok542 283.469.88 (n 10), and dao-5(ok542); cguIs13 448.620.22 (n 5). For post-L4 24 h, N2 480.254.3 (n 4), dao-5(ok542) 336.857.29 (n 11),

dao-5(ok542); cguIs13 46317.8 (n 7). For post-L4 12 h, N2 versus dao-5(ok542) and dao-5(ok542); cguIs13 versus dao-5(ok542); and post-L4 24 h, N2 versus

dao-5(ok542) and dao-5(ok542); cguIs13 versus dao-5(ok542), ***Po0.001. (d) Germ cell apoptosis in worms with wild-type background (bcIs39) or dao-5 mutation (dao-5(ok542); bcIs39). The reporter transgene bcIs39, whose dying cells were decorated with CED-1::GFP, were used to facilitate the counting. Representative micrographs of the two strains are shown in the upper panel. Note that the occurrence of CED-1::GFP-surrounded cells signal in the bcIs39; ok542 is more than that of bcIs39 background. Bar represents 40 mm. Lower panel, the graphic representation of the quantitation of CED-1::GFP decorated cells counted in bcIs39 (n 36) or dao-5(ok542); bcIs39 (n 56).

The X axis indicates the numbers of dying cells and the Y axis indicates the numbers of gonad arms observed

decreased in dao-5(ok542) mutants as compared with wild-type N2 animals, suggesting that DAO-5 activity is correlated to the activeness of rDNA chromatin (Figure 5b). As rDNA chromatin status could be dynamic,33,34 we next checked

whether the inactiveness of rDNA chromatin of dao-5(ok542) would be also increased correspondingly. As expected, the di-methylated histone lysine 9 of histone H3 (H3K9me2) level, an inactive mark, in dao-5(ok542) was drastically increased ve times compared with the low level of H3K9me2 in N2 (Figure 5c), suggesting that the absence of DAO-5 affects the active level around the rDNA promoter. On the other hand, the levels of another inactive mark, trimethylated histone lysine 9 of histone H3, H3K9me3, appeared insignicantly different between N2 and dao-5(ok542) animals (Figure 5d). Interestingly, the distinct proles of two inactive histone marks, H3K9me2 and H3K9me3, around the rDNA promoter between N2 and dao-5(ok542) worms might reect that there are distinct species of C. elegans rDNA (see Discussion). By and large,

these ChIP results suggest that DAO-5 is important to maintain the active chromatin status of the rDNA promoter to accommodate the transcribing Pol I machinery, thereby facilitating rDNA transcription.

CEP-1/p53 activity was elevated in the dao-5(ok542) mutant. From the data above, it could be informed that the absence of DAO-5 affects rDNA transcription accompanying the gonadal defects. To cope with malfunctioning or damaged ribosome biogenesis, a p53-responsive mechanism termed ribosomal stress or nucleolus stress has been long observed in mammals.1 Previously, in C. elegans, several lines of evidence showed that the disrupted ribosomal biogenesis or depletion of nucleolar proteins would induce CEP-1 (the C. elegans p53 homolog) activity to enhance defensive or protective mechanisms in the organism.35,36 To examine whether loss of DAO-5 would also elicit a higher CEP-1 activity, we rst performed reverse transcription-quantitative PCR (RT-qPCR) to determine the

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Figure 4 The absence of DAO-5 impairs the rDNA transcription efcacy. (a) In situ run-on assays were performed in the derived embryonic neuromuscular cells. Detection of Br-UTP incorporation (stained in red) is shown in the second column and the localization of DAO-5 (stained in green) is shown in the rst column. The third column is merged from images of the rst and the second column (shown in yellow), whereas the DNA counterstaining with Hoechst 33342 is shown in the fourth column. Note that the Hoechst 33342-negative region in the nuclei is the site of the nucleoli because the nucleolus has a high abundance of RNA but less DNA. Scale bar indicates 5 mm. (b) Quantitative run-on assay followed by dot-blot analysis with isolated cells from the larvae of N2 and dao-5(ok542) animals. The left panel shows the blots from three independent experiments and the quantitated relative densitometry data from three blots are shown in the right panel. *Po0.05 in paired t-test

abundance of egl-1 and ced-13 transcripts,3739 both CEP-1

downstream target genes whose induction are regarded as CEP-1 activation, in N2 and dao-5(ok542) animals. The amounts of egl-1 and ced-13 transcripts were 2- to 6-fold higher in dao-5(ok542) worms compared with N2 (Figure 6a). Furthermore, ChIP assays also conrmed that an increased mRNA abundance was a CEP-1-mediated transcription regulation as the occupancies of CEP-1 on the egl-1 and ced-13 gene promoters were higher in dao-5 background

compared with that of N2 animals (Figures 6b and c). Taken together, CEP-1 activation is suggested to be responsive to the absence of DAO-5.

Discussion

The importance of DAO-5 during germline development. In addition to two reports by Hadwiger et al.21 and Korcekova et al.,22 in this study, we have shown that DAO-5 of

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a Pol l/rDNA promoter

H3K9me2/rDNA promoter H3K9me3/rDNA promoter

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Figure 5 The absence of DAO-5 attenuates Pol I occupancy and alters the modications of histones around the rDNA promoter. (a) The ChIP assays show that the occupancy of RNA Pol I in the rDNA promoter in dao-5(ok542) animals is weaker than that of N2. The average relative binding ratio is shown. The error bars represent S.D., n 5. *Po0.05 in paired t-test. (b) The level of acetylated histone

H4 (H4ac), a mark for open and actively transcribed chromatin, on rDNA promoter was found signicantly decreased in ok542 than in N2. Error bars represent the S.D., n 4. *Po0.05. (c) The inactive mark H3K9me2 level was signicantly

increased in dao-5(ok542) compared with that in N2. Error bars represent S.D., n 6 in N2, n 3 in dao-5(ok542). N2 versus dao-5(ok542), ***Po0.001. (d) The

difference in the level of inactive mark H3K9me3 between N2 and dao-5(ok542) was not signicant. Error bars represent S.D., n 6 in N2, n 4 in dao-5(ok542). No

signicance (NS) between N2 and dao-5(ok542)

C. elegans is a member of Nopp140 family, a conserved nucleolar protein across metazoans (Figures 1 and 2). DAO-5/CeNopp140 is important for sustaining germline development, particularly oogenesis. In the absence of DAO-5, worms exhibited severe defects in oogenesis together with increased germ cell apoptosis and became semi-infertile (Figure 3). DAO-5 deciency does not cause severe effects on tissue development until the L4 stage wherein active oogenesis emerges. As an energy-demanding process that costs a large amount of proteins and RNA, oogenesis seems more sensitive to ribosome inadequacy that fails to meet the requirement during oocyte maturation. As no notable defects were found in the spermatheca in dao-5(ok542) hermaphrodites and males (data not shown), the fertility defect of dao-5 mutants seems only attributed to the oogenesis. The gonadal defects observed in the absence of DAO-5 are also reminiscent of the phenotypes observed in pro (proximal tumor in gonad) mutants, whose ribosome

production is also disrupted,40 although their underlying mechanism may differ. Sheath cells, a specialized somatic tissue consisting of ve pairs of at cells that surround the germline, are crucial to coordinate germline development.41

Impairments of gonadogenesis that occurred in pro-1, pro-2, and pro-3 mutants are considered the result of the affected sheath cells in terms of lower cell number, particularly, in a nonautonomous manner.40 We, however, are inclined to the view that the gonadal defects observed in DAO-5 deciency are cell autonomous based on two lines of observation. First, the number of sheath cells around the gonad was not reduced in the absence of DAO-5 (data not shown). Second, the oogenic defect in a dao-5 mutant was rescued by germline expression of DAO-5::GFP (Figures 3a and c) but not a high-copy extrachromosomal array (data not shown) that was only expressed in somatic gonadal cells including sheath cells (Figure 2b). Taken together, DAO-5 is essential for normal germline development, especially oogenesis, in a cell-autonomous manner.

Implication of DAO-5/CeNopp140 functioning to control the rDNA chromatin status. The importance of Nopp140 in rDNA transcription level has been revealed previously.9,13 In

the present study, we demonstrated that DAO-5/CeNopp140 plays a conserved role in a complex containing RNA Pol I and rDNA as shown in mammals. Loss of DAO-5 results in inefcient rDNA transcription (Figure 4) that may help explain a recent observation with decreased abundance of pre-rRNA in DmNopp140-depleted Drosophila.42 Furthermore, our current study is the rst demonstration that DAO-5/CeN-opp140 is important to maintain the active chromatin status of rDNA (Figures 5bd). In DAO-5-decient worms, histone modication patterns on the rDNA promoter chromatin are altered dramatically, shifting from H4ac enriched to H3K9me2 deposition. Such a dynamic change implicates that the loss of DAO-5 renders the rDNA chromatin less active, thus compromising the rDNA transcription. On the other hand, H3K9me3 level, which is another inactive marker, does not display an increase in the absence of DAO-5. We speculate that the invariant H3K9me3 modication around rDNA may reect the existence of the permanently dormant moiety in C. elegans rDNA, as revealed in mammals.43

How DAO-5 plays a role in controlling the rDNA transcription machinery for optimizing rRNA production is unknown. As Nopp140 serves as a nucleolar scaffold for recruiting Pol I apparatus to arrange rDNA cluster properly,9,13 whether there is involvement of histone-modifying enzymes with DAO-5/CeNopp140, such as histone acetyltransferase (HAT) or histone demethylase (KDM), acting in concert to maintain an active rDNA chromatin status is an attractive hypothesis. For example, a histone H3K9 demethylase, PHF8, activates rDNA transcription by H3K91/2 demethylation.44

Strikingly, a point mutation within PHF8 gene that abolishes its demethylating ability has been identied as well as a causal conjunction to another ribosomopathy, X-linked mental cleft/plate defects.45 Therefore, the participation of histone-modifying enzymes that may potentiate in rDNA modulation of Nopp140 remains to be explored.

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Figure 6 The CEP-1-mediated transactivation in the absence of DAO-5. (a) The abundance of transcripts of egl-1 and ced-13 (two downstream genes of cep-1) in N2 and dao-5(ok542) worms were compared by RT-qPCR. The average relative expression folds are shown. Error bars represent S.D, n 3 in egl-1 and n 4 in ced-13. *Po0.05 in

paired t-test. (b) The ChIP assay showed that the CEP-1 occupancies on the gene promoters of (b) egl-1 or (c) ced-13 was higher in dao-5(ok542) than in N2. The average binding ratios are shown. Error bars represent S.D., n 3. *Po0.05 in paired t-test

CEP-1/p53-mediated ribosomal stress. Many studies have established p53 as the stress hub responsive to defective ribosome biogenesis (for review, see Boulon et al.1). In a TCS mouse model, p53 activation is a hallmark and is regarded as the principal cause for neuroepithelial apoptosis.46 In this study with the C. elegans model, we provided evidence that both CEP-1 target genes, egl-1 and ced-13, each encoding a key activator of apoptosis, would be transactivated in the absence of DAO-5 as shown in other stresses, such as genotoxic response (Figure 6).3739 Thus, the higher apoptotic rate

found in the absence of DAO-5 (Figure 3d) seems to be conserved with the TCS murine model. Although the underlying CEP-1/p53-triggering mechanism in the absence of DAO-5/CeNopp140 remains obscure, the increase in apoptosis may serve as a protective surveillance in C. elegans gonad to prevent the nonqualied germ cells from giving rise to oocytes. Of note, oogenesis progression in C. elegans gonad, as in other species, is a G2/M transition. In mammalian contexts, however, the p53-mediated transactivation during ribosomal stress usually lead to the cell cycle arrest at the G1/S phase.47 Interestingly, two recent studies also observed the presence of p53-mediated G2/M blockade during the induced ribosomal stress in cultured cells.48,49

Therefore, C. elegans gonad may provide a platform to study the novel link of CEP-1/p53-mediated ribosomal stress with G2/M block.

In summary, results reported here have demonstrated a novel role of DAO-5/CeNopp140 in rDNA transcription and have linked its functionality with an important developmental process, oogenesis (Figure 7). The loss of DAO-5 induces ribosomal stress in terms of the activated cep-1 transactivation to cause additional germ cell apoptosis. We thus suggest that C. elegans is a potentially valuable model for studying human ribosomopathy-associated diseases, given that most human genes related to ribosomopathy have been identied to have corresponding equivalents in C. elegans.50 In the

future, a detailed mechanism of ribosomopathy at the molecular and cellular levels might be elucidated withinC. elegans.

Materials and MethodsStrain maintenance. All strains were maintained with standard procedures and raised at 201C.51 Bristol N2 was used as a wild-type animal. The dao-5(ok542) homozygote was segregated from a balanced heterozygote VC340 from

C. elegans Gene Knockout Consortium (Oklahoma City, OK, USA). Four times of backcrossing to N2 were done before the phenotypic examination. The PCR primers used for genotyping were as follows: ok542_external_F: 50-GATTG

GTTGATTGGACCACC-30, ok542_external_R: 50-TGAGTTCCGACTTGTATGCG-30; ok542_internal_F: 50-TTTCACAAAGAAACCCGGAG-30, ok542_internal_R: 50-CAGTCGAGGTAGCCAATGGT-30; and the ok542_internal_third primer: 50-CTCGAGGTTACTCCAGTTGCGAAT-30. MD701 (bcIs39 [Plim-7::ced-1::gfp;lin-15( )]) background was used to evaluate germ cell apoptosis.29 In the early

phase of this study, N2 worms were provided by Yu-Chun Wu (National Taiwan University, Taipei, Taiwan). The other strains were then obtained from the Caenorhabditis Genetics Center (University of Minnesota, Twin Cities (Minneapolis and St. Paul), MN, USA).

Constructs and transgenics. Two DAO-5::GFP translational fusion transgenes with different expression cassettes were created in this study. For the Pdao-5::dao-5::gfp-expressing (DAO-5::GFP) construct, both 1498-bp dao-5 gene promoter fragment and 3106-bp genomic DNA fragment were subsequently cloned into pPD95.75 (Addgene, Cambridge, MA, USA). The resulting transgenic line created by microinjection exists as an extrachromosomal array.52 To express exogenous DAO-5 in the germline, a pie-1-driven DAO-5::GFP expression cassette (Ppie-1::dao-5::gfp::30UTRpie-1) was generated with Multisite Gateway cloning (Invitrogen, Carlsbad, CA, USA).53 The resulting integration line (designated as cguIs13) was established with the microparticle bombardment technique54 and outcrossed once to remove potentially hidden mutations. Both constructs were veried and sequenced before being subjected to transformation.

Immunoprecipitation and western blotting. The crude lysates were prepared with young adult animals in PRO-PREP lysis buffer (iNtRON, Seongnam, South Korea) supplemented with a complete protease inhibitor cocktail (Roche, Basel, Switzerland) by sonication. After centrifugation (11 000 g, 4 1C, 10 min),

the supernatants were collected and protein concentrations were determined by standard Bradford assay (Bio-Rad, Hercules, CA, USA). The lysate containing 2 mg of proteins was used to incubate with 4 mg of RPA194 antibody (sc-28714,

Santa Cruz, Dallas, TX, USA) for 12 h at 41C. The resulting immunocomplex was bound and precipitated with 50 ml protein A/G plus agarose beads (Santa Cruz) for 1 h. The beads were washed three times with NET buffer (50 mM Tris HCl, pH 7.5, 5 mM EDTA, 150 mM NaCl, 0.5% NP-40) and boiled in Laemmli sample buffer for 10 min. After 10 min of centrifugation (12 000 g, 41C), lysate suspensions of the

respective sample were analyzed in 8% SDS-PAGE. Proteins were transferred to a PVDF membrane and the resulting blots were detected with the primary antibodies as indicated. The DAO-5-specic monoclonal antibody 5E9 (Developmental Studies Hybridoma Bank, Iowa City, IA, USA)21was used in 510 times

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Figure 7 A working model of DAO-5 regulation in oogenesis. In the wild-type animal (N2), DAO-5 maintains the epigenetically active rDNA chromatin to facilitate rDNA transcription and sustain germline development (left scheme). Once DAO-5 is absent, rDNA transcription is hampered as rDNA becomes inaccessible because of H3K9me2 enrichment and reduced H4ac modication on nucleosomes that thereby results in alteration of rRNA synthesis and subsequently induces CEP-1-mediated ribosomal stress in terms of the increased germ cell apoptosis and impairment of oogenesis (right scheme). HAT, histone acetyltransferase; KDM, histone demethylase

dilution with 5% skim milk/PBST (0.5% Tween-20). The blots were developed and detected with chemiluminescence ECL kit (T-Pro Biotechnologies, New Taipei City, Taiwan).

Immunostaining, image acquisition, and quantitative image analyses. The global DAO-5::GFP expression pattern (Figure 2a) was acquired with a Zeiss LSM 510 Meta confocal microscope (Jena, Germany). To facilitate immunostaining, gonads were protruded by decapitating 1-day-old adult animals with 25-gauge needles and xed with 1% formaldehyde. The xed gonads (attached to the carcasses) were preincubated with 0.1% BSA/PBST and then stained with the anti-brillarin (1 : 500; Novus Biologicals, NB300-269, Littleton, CO, USA) and secondary antibody conjugated Alexa 594 (1 : 1000; Molecular Probes, Eugene, OR, USA). Images were captured with a microscope (Leica DM2500, Wetzlar, Germany) coupled with CoolSNAP K4 CCD (Photometrics, Tucson, AZ, USA) and MetaMorph software (MDS Analytical Technologies, Sunnyvale, CA, USA). For monitoring gonadal extension, the animals at their corresponding stages were collected and stored in 1 MRWB (80 mM KCl,

20 mM NaCl, 10 mM disodium EGTA, 5 mM spermidine, 15 mM PIPES, pH 7.4, 25% methanol, 1.6% formaldehyde) at 801C until staining. The xed animals

were stained with Hoechst 33342 (Molecular Probes) to highlight nuclear DNA. As the gonadal tissues are mainly composed of the morphologically distinct nuclei, the overall outline and length of the developing gonads could be determined with microphotography. Images were acquired as described above and analyzed with Metamorph.

Apoptosis assessment. The reporter strain bcIs39 Plim-7::ced-1::gfp; lin-15( )] was used to generate bcIs39;ok542 to facilitate the counting of dying

germ cells.29 Living animals (B24 h post L4 stage) were mounted and anesthetized on agar pads and examined with microscopy as described above.

In situ and quantitative run-on assay (Br-UTP incorporation). Procedures for conducting primary culture of C. elegans embryonic cells were adopted from Strange et al.55 In brief, the C. elegans embryos were collected by hypochlorite lysis of gravid worms, and then treated with chitinase (2 U/ml, Sigma-Aldrich, St. Louis, MO, USA) at room temperature for 20 min to remove the eggshell. Following gentle trituration through a plastic 1-ml pipet tip and ltration through a 5-mm Durapore lter, the dissociated single cells were cultured in L-15 medium supplemented with 10% (v/v) heat-inactivated fetal bovine serum (Gibco, Gaithersburg, MD, USA), 50 U/ml penicillin, and 50 mg/ml streptomycin (Sigma-Aldrich) on glass coverslips coated with peanut lectin (Sigma-Aldrich) at

241C in a humidied atmosphere. The attached cells were subjected to in situ transcription assay after 1 day of settlement.

In situ run-on assays were performed as described previously,9,13 with few

modications. Briey, cells were permeabilized by ice-cold digitonin (150 mg/ml; Sigma-Aldrich) and were incubated with 1 transcription PB buffer (22 mM NaCl,

1 mM MgCl2, 8 mM KCl, 11 mM K2 HPO4, 100 mM CH3COOK, 1 mM ATP, 1 mM DTT) containing NTPs mixture (Roche) and 0.2 mM Br-UTP (Sigma-Aldrich). The run-on transcription was carried out at 241C for the indicated pulsing time (5 or 30 min), and terminated by rinsing the coverslips in ice-cold PBS. The nascent

RNAs labeled by Br-UTP were visualized by immunouorescence staining with anti-BrdU antibody conjugated with Alexa Fluor 594 (Molecular Probes) and DAO-5 was stained with a rabbit polyclonal antibody CSK-14.

To quantify the Br-UTP incorporation, isolated larval cells from N2 and dao-5(ok542) animals were used as described by Zhang et al.56 Briey, B100 ml packed

L4 larvae (precleared of bacteria by staying in egg buffer (118 mM NaCl, 48 mM KCl, 2 mM CaCl2, 2 mM MgCl2, 25 mM HEPES, pH 7.3) for 1 h) were treated with 600

800 ml SDS-DTT solution to disrupt cuticle, and the subsequent digestion with B300 ml of pronase (15 mg/ml, Sigma-Aldrich), combined with mechanical disruption (200250 strokes with a 200 ml tip) to release cells. After the debris was settled down, the oating dissociated cells were collected and examined under an inverted microscope (Olympus IX-71, Tokyo, Japan). The cells were pelleted and resuspended in 90 ml PB buffer supplemented with digitonin (150 mg/ml), a-amanitin (5 mg/ml), and RNase OUT (400 U/ml, Invitrogen) for preincubation at room temperature for 10 min. Following preincubation, 10 ml of 10X transcription mix with

Br-UTP was added. After the 30-min pulsing period, the run-on reactions were terminated with adding 1 ml Trizol reagent (Invitrogen). RNAs were extracted with Trizol purication according to the manufacturers instruction and resuspended in 20 ml of water.

Next, 2 ml of the total extracted RNAs (namely the run-on products) were applied onto a nylon membrane (GeneScreen Plus, PerkinElmer, Boston, MA, USA), UV cross-linked (Spectroline, Westbury, NY, USA), and then subjected to immunodetection. Br-UTP incorporated RNAs were detected with a sheep anti-BrdU antibody (1 : 1500, ab1893; Abcam, Cambridge, UK) and rabbit anti-sheep secondary antibody (1 : 3500) in 1% skim milk in TBST (0.5% Tween-20). The signals were developed and detected with chemiluminescence ECL kit (T-Pro Biotechnologies). The integrated intensities of dot blots were measured with MetaMorph software and calibrated with actin mRNA level (determined by RT-qPCR).

Chromatin immunoprecipitation. ChIP assays were performed using animals at L4 stage of the respective genotypes as previously described.57 Briey,

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chromatin lysates were prepared from 1% formaldehyde-crosslinked animals and then sonicated to shear the chromatin DNA to a length of 500800 bp. For determining DAO-5 occupancy, 50 ml supernatant of 5E9 hybridoma culture was used for each ChIP to incubate with the chromatin lysate (1 mg proteins). For ChIP assays with epigenetic marks, 2 mg of different antibodies, anti-H4ac (06598,

Millipore, Billerica, MA, USA), anti-H3K9me2 (ab1220, Abcam), or anti-H3K9me3 (ab8898, Abcam), were added into the lysate solution. For probing Pol I occupancy, 4 or 8 mg of anti-RPA194 antibodies (sc-28714, Santa Cruz) were coincubated with lysate. The protein A/G beads (sc-2003, Santa Cruz) were used as a precipitant of the immunocomplex. The chromatin immunoprecipitates were washed, de-crosslinked, and recovered. The abundance of genes was detected by quantitative PCR with SsoFast EvaGreen Supermix and iQ5 cycler (Bio-Rad). Oligonucleotides used in this study were as follows:rDNA promoter: F 50-GTGTTGGTGATGGTAGTGTGTG-30 (587608) and R 50-CGGCGCAATGATATAAAGAACTCG-30 (694717);

26S gene body: F 50-GGAGTGCTTGTCTACTGCGAG-30 (43814401) and R 50-CCTCTGCACAGTCACAAGTG-30 (4531);rDNA terminator: F 50-TTTCCTTTTCCTACACTCATGTC-30 (123) and R 50-CCCTTCACCAGCCTCTGAAT-30 (190209);b-1 promoter: F 50-AGATCGACTGGAGCGTGATT-30 and R 50-GGGAGAGCC GAGTAAGATTG-30

5S rRNA gene promoter: F 50-CGAGGTCTACGATCGGCAAC-30 R 50-GTCTAT GGACAAGTCCCATG-30egl-1 promoter: F 50-ACACTTCAAGAGCTATGAGTTTGTC-30 and R CGAACGT TTTCGAAACGG-30;

ced-13 promoter: F 50-GTTTCTGTCCGCCTTCCTT-30 and R 50-GTCGG TTATCGGTGAAACTGTA-30.

Reverse transcription and quantitative PCR. The total RNAs of the indicated staged worms were extracted with Trizol (Invitrogen). The integrity of the RNA was inspected by 1% agarose gel analysis and the concentrations of the RNAs were determined with Nanovue (GE Healthcare, Uppsala, Sweden). Then, 1 mg of the total RNA was converted into cDNA with iScript cDNA synthesis kit (Bio-Rad). qPCR was performed with SsoFast

EvaGreen Supermix in iQ5 cycler (Bio-Rad) following the standard protocol: egl-1_coding region: F TACTCCTCGTCTCAGGACTT-30 and R CATCGAAGT

CATCGCACAT-30;

ced-13_coding region: F 50-TGATGTCGTACAAGCGTGAT-30 and R 50-AAAAA ACACGACGAACAATGCTGG-30;

actin: F 50-TCGGTATGGGACAGAAGGAC-30 and R 50-CATCCCAGTTGGTGA CGATA-30.

Conict of InterestThe authors declare no conict of interest.

Acknowledgements. We thank Caenorhabditis Genetics Center (University of Minnesota), C. elegans Gene Knockout Consortium (University of British Columbia), and Yi-Chun Wu (National Taiwan University) for providing various strains of worms. We thank Scott C Schuyler (Chang Gung University) for critical reading and English editing of the manuscript. We also thank the microscope core facility of MMRC at Chang Gung University for providing the services and Yung-Hsiang Yi (Chang Gung University) for consulting on the dot-blot quantitation. This work was supported by grants (EMRPD18031, EMRPD190071, and EMRPD1A0431) from the Ministry of Education and (CMRPD160011-3) from the Chang Gung Memorial Hospital to SJL.

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