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Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes

Authors :
Atsushi Hattori
Atsuhito Seki
Naoto Inaba
Kazuhiko Nakabayashi
Kazue Takeda
Kuniko Tatsusmi
Yasuhiro Naiki
Akie Nakamura
Keisuke Ishiwata
Kenji Matsumoto
Michiyo Nasu
Kohji Okamura
Toshimi Michigami
Yuko Katoh-Fukui
Akihiro Umezawa
Tsutomu Ogata
Masayo Kagami
Maki Fukami
Source :
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Publication Year :
2024
Publisher :
Nature Portfolio, 2024.

Abstract

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.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
20452322
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Scientific Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.3019d22edd4d4c8dbe4a7506cd74d8be
Document Type :
article
Full Text :
https://doi.org/10.1038/s41598-024-58530-9