Possible role of USP26 in patients with severely impaired spermatogenesis

被引:71
作者
Stouffs, K
Lissens, W
Tournaye, H
Van Steirteghem, A
Liebaers, I
机构
[1] Free Univ Brussels, Dutch Speaking Brussels Free Univ, Univ Hosp, Ctr Med Genet, B-1090 Brussels, Belgium
[2] Free Univ Brussels, Dutch Speaking Brussels Free Univ, Univ Hosp, Ctr Reprod Med, B-1090 Brussels, Belgium
关键词
USP26; male infertility; Sertoli cell-only syndrome; X chromosome;
D O I
10.1038/sj.ejhg.5201335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ubiquitin-specific protease 26 (USP26) gene is an X-linked gene specifically expressed in testis tissue. This gene is therefore a potential infertility gene. In order to analyse its possible involvement in spermatogenesis and infertility, 42 patients with Sertoli cell-only syndrome were analysed for mutations in this gene. We found four patients with exactly the same three changes of the nucleotide and therefore also amino acid sequence. These patients showed 370-371insACA, 494>4C and 1423C>T causing T123-124ins, L165S and H475Y, respectively. These changes were not found in 10 control samples. Furthermore, two polymorphisms were observed which do not alter the amino-acid sequence. A restriction analysis that can make a distinction between a T and a C, at position 494, was set up in order to examine more patient and control samples. Another 69 patients with Sertoli cell-only syndrome, 32 patients with maturation arrest and 142 control samples were analysed using this method. None of the control samples or patients with maturation arrest featured the change at position 494. However, four more patients with Sertoli cell-only syndrome were identified with the three alterations. The frequency of alterations in this group is therefore 7.2% (8/111). One of the patients had a deletion of the long arm of the Y chromosome, while another patient had a varicocoele. These results indicate that these alterations might be involved in male infertility or might increase the risk of male infertility.
引用
收藏
页码:336 / 340
页数:5
相关论文
共 8 条
  • [1] Specific aspects of the ubiquitin system in spermatogenesis
    Baarends, WM
    van der Laan, R
    Grootegoed, JA
    [J]. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2000, 23 (09) : 597 - 604
  • [2] The ubiquitin system in gametogenesis
    Baarends, WM
    Roest, HP
    Grootegoed, JA
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 151 (1-2) : 5 - 16
  • [3] The possible biological and reproductive functions of ubiquitin
    Bebington, C
    Doherty, FJ
    Fleming, SD
    [J]. HUMAN REPRODUCTION UPDATE, 2001, 7 (01) : 102 - 111
  • [4] Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and manning to the Sxrb interval of the mouse Y chromosome of the Dffry gene
    Brown, GM
    Furlong, RA
    Sargent, CA
    Erickson, RP
    Longepied, G
    Mitchell, M
    Jones, MH
    Hargreave, TB
    Cooke, HJ
    Affara, NA
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (01) : 97 - 107
  • [5] Impact of genetic engineering on the understanding of spermatogenesis
    Escalier, D
    [J]. HUMAN REPRODUCTION UPDATE, 2001, 7 (02) : 191 - 210
  • [6] GREENHALL E, 1990, FERTIL STERIL, V54, P978
  • [7] Male infertility
    Iammarrone, E
    Balet, R
    Lower, AM
    Gillott, C
    Grudzinskas, JG
    [J]. BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY, 2003, 17 (02) : 211 - 229
  • [8] An abundance of X-linked genes expressed in spermatogonia
    Wang, PJ
    McCarrey, JR
    Yang, F
    Page, DC
    [J]. NATURE GENETICS, 2001, 27 (04) : 422 - 426