Abstract

All attempts to identify male-specific growth genes in humans have failed. This study aimed to clarify why men are taller than women. Microarray-based transcriptome analysis of the cartilage tissues of four adults and chondrocytes of 12 children showed that the median expression levels of SHOX, a growth gene in the pseudoautosomal region (PAR), were higher in male samples than in female samples. Male-dominant SHOX expression was confirmed by quantitative RT-PCR for 36 cartilage samples. Reduced representation bisulfite sequencing of four cartilage samples revealed sex-biased DNA methylation in the SHOX-flanking regions, and pyrosequencing of 22 cartilage samples confirmed male-dominant DNA methylation at the CpG sites in the SHOX upstream region and exon 6a. DNA methylation indexes of these regions were positively correlated with SHOX expression levels. These results, together with prior findings that PAR genes often exhibit male-dominant expression, imply that the relatively low SHOX expression in female cartilage tissues reflects the partial spread of X chromosome inactivation into PAR. Altogether, this study provides the first indication that sex differences in height are ascribed, at least in part, to the sex-dependent epigenetic regulation of SHOX. Our findings deserve further validation.

Details

Title
Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes
Author
Hattori, Atsushi 1 ; Seki, Atsuhito 2 ; Inaba, Naoto 2 ; Nakabayashi, Kazuhiko 3 ; Takeda, Kazue 4 ; Tatsusmi, Kuniko 5 ; Naiki, Yasuhiro 6 ; Nakamura, Akie 7 ; Ishiwata, Keisuke 3 ; Matsumoto, Kenji 4 ; Nasu, Michiyo 5 ; Okamura, Kohji 8 ; Michigami, Toshimi 9 ; Katoh-Fukui, Yuko 7 ; Umezawa, Akihiro 5 ; Ogata, Tsutomu 10 ; Kagami, Masayo 7 ; Fukami, Maki 1 

 National Research Institute for Child Health and Development, Department of Molecular Endocrinology, Tokyo, Japan (GRID:grid.63906.3a) (ISNI:0000 0004 0377 2305); National Research Institute for Child Health and Development, Division of Diversity Research, Tokyo, Japan (GRID:grid.63906.3a) (ISNI:0000 0004 0377 2305) 
 National Medical Center for Children and Mothers, Department of Orthopaedic Surgery, Tokyo, Japan (GRID:grid.416239.b) 
 National Research Institute for Child Health and Development, Department of Maternal-Fetal Biology, Tokyo, Japan (GRID:grid.63906.3a) (ISNI:0000 0004 0377 2305) 
 National Research Institute for Child Health and Development, Department of Allergy and Clinical Immunology, Tokyo, Japan (GRID:grid.63906.3a) (ISNI:0000 0004 0377 2305) 
 National Research Institute for Child Health and Development, Center for Regenerative Medicine, Tokyo, Japan (GRID:grid.63906.3a) (ISNI:0000 0004 0377 2305) 
 National Medical Center for Children and Mothers, Division of Endocrinology and Metabolism, Tokyo, Japan (GRID:grid.416239.b) 
 National Research Institute for Child Health and Development, Department of Molecular Endocrinology, Tokyo, Japan (GRID:grid.63906.3a) (ISNI:0000 0004 0377 2305) 
 National Research Institute for Child Health and Development, Department of Systems BioMedicine, Tokyo, Japan (GRID:grid.63906.3a) (ISNI:0000 0004 0377 2305) 
 Osaka Prefectural Hospital Organization, Department of Bone and Mineral Research, Research Institute, Osaka Women’s and Children’s Hospital, Izumi, Japan (GRID:grid.416629.e) (ISNI:0000 0004 0377 2137) 
10  Hamamatsu University School of Medicine, Department of Pediatrics, Hamamatsu, Japan (GRID:grid.505613.4) (ISNI:0000 0000 8937 6696); Hamamatsu Medical Center, Department of Pediatrics, Hamamatsu, Japan (GRID:grid.413553.5) (ISNI:0000 0004 1772 534X) 
Pages
8069
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3033763209
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.