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Mutations in SOHLH1 gene associate with nonobstructive azoospermia

Authors
 Youngsok Choi  ;  Sanghyun Jeon  ;  Mikyung Choi  ;  Min-ho Lee  ;  Miseon Park  ;  Dong Ryul Lee  ;  Kyu-Yeon Jun  ;  Youngjoo Kwon  ;  Ok-Hee Lee  ;  Seung-Hun Song  ;  Ji-Young Kim  ;  Kyung-Ah Lee  ;  Tae Ki Yoon  ;  Aleksandar Rajkovic  ;  Sung Han Shim 
Citation
 HUMAN MUTATION, Vol.31(7) : 788-793, 2010 
Journal Title
 HUMAN MUTATION 
ISSN
 1059-7794 
Issue Date
2010
MeSH
Adult ; Amino Acid Sequence ; Azoospermia/genetics* ; Base Sequence ; Basic Helix-Loop-Helix Transcription Factors/genetics* ; Cell Line ; DNA Mutational Analysis ; Exons/genetics ; Female ; Gene Deletion ; Genetic Predisposition to Disease* ; Humans ; Introns/genetics ; Luciferases/genetics ; Luciferases/metabolism ; Male ; Molecular Sequence Data ; Mutation* ; Pedigree ; Polymorphism, Single Nucleotide ; RNA Splice Sites/genetics ; Sequence Homology, Amino Acid ; Testis/metabolism ; Testis/pathology ; Transfection
Keywords
nonobstructive Azoospermia ; NOA ; SOHLH1 ; testis ; spermatogenesis
Abstract
In a previous study, we found SOHLH1 (spermatogenesis and oogenesis-specific basic helix-loop-helix 1) as the first testis-specific basic helix-loop-helix transcription factor essential for spermatogonial differentiation. SOHLH1 therefore represents an excellent candidate gene for testicular failure such as nonobstructive azoospermia (NOA). We analyzed whether there were mutations in the SOHLH1 gene in 96 Korean patients with NOA. The sequence analysis discovered three novel variations: one intronic variant (c.346-1G>A), and two nonsynonymous exonic variants (c.91T>C and c.529C>A) with known single nucleotide polymorphisms (SNPs), which included six intronic variants, two synonymous, and two nonsynonymous variants. We examined the consequences of mutations in SOHLH1 using in vivo and in vitro assays. Analysis of transcripts from minigenes carrying the c.346-1G>A revealed that splicing site variation leads to the partial deletion at a cryptic splicing site within exon 4. This deletion results in SOHLH1 with a truncated bHLH domain. Transient transfection assay showed that the SOHLH1 mutant with the truncated domain disrupted the transcriptional activity of KIT promoter, whereas two missense mutations harboring either p.Arg37Gln or p.Pro269Ser did not have a significant effect on its transactivation. Our findings indicate that a splice-acceptor site mutation that probably causes a nonfunctional SOHLH1 protein results in nonobstructive azoospermia by the lack of normal spermatogenesis.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/humu.21264/abstract
DOI
10.1002/humu.21264
Appears in Collections:
5. Research Institutes (연구소) > Yonsei Integrative Research Institute for Cerebral & Cardiovascular Disease (뇌심혈관질환융합연구사업단) > 1. Journal Papers
Yonsei Authors
Lee, Ok Hee(이옥희)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/102379
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