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DAZ基因家族与男性不育的研究进展 被引量:3

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摘要 据WTO调查显示正常育龄夫妇中约10%~15%患有不孕症,由男性因素引起的不育约占50%。近年来的研究发现Y染色体长臂无精症因子(azoospermiafactor,AZF)的微缺失是导致男性不育的一个重要病因。其中DAZ(the deleted in azoospermia)基因为AZFc区的候补基因,和DAZL(deleted in azoospermia-like)、BOULE同属于DAZ基因家族,其编码的蛋白均为RNA结合蛋白,含有高度保守的RNA结合域(RNA binding domain,RBM)和DAZ重复(DAZ repeat)序列,且均在生殖细胞中特异表达,参与调节生殖细胞的发育和分化。本文旨在对DAZ基因家族成员的生理功能以及与男性不育的关系作一综述。
机构地区 汕头大学医学院
出处 《国际泌尿系统杂志》 2009年第1期70-73,共4页 International Journal of Urology and Nephrology
基金 广东省自然科学基金项目(No.06027982)
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  • 1Liu J, Nagy Z, Joris H, Tournaye H, Devroey P, Van Steirteghem A. Successful fertilization and establishment of pregnancies after intracytoplasmic sperm injection in patients with globozoospermia. Hum Reprod 1995; 10: 626-9.
  • 2Hoos A, Cordon-Cardo C. Tissue microarray profiling of cancer specimens and cell lines: opportunities and limitations. Lab Invest 2001; 81: 1331-8.
  • 3Kononen J, Bubendorf L, Kalliortiemi A, Barltmd M, Schraml P, Leighton S, et al. Tissue microarrays for high-throughput molecular profiling of tumor specimens. Nat Med 1998; 4:844-7.
  • 4Wang H, Zhang W, Fuller GN. Tissue microarrays: applications in neuropathology research, diagnosis, and education. Brain Pathol 2002; 12: 95-107.
  • 5Horvath L, HenshaU S. The application of tissue microarrays to cancer research. Pathology 2001; 33:125-9.
  • 6Baker HW. Management of Male Infertility. Baillieres Best Pract Res Clin Endocrinol Metab 2000; 14: 409-22.
  • 7McLachlan RI, Mallidis C, Ma K, Bhasin S, de Kretser DM.Genetic disorders and spermatogenesis. Reprod Ferfil Dev 1998;10: 97-104.
  • 8Kim ED, Bischoff FZ, Lipshultz LI, Lamb DJ. Genetic concerns for the subfertile male in the era of ICSI. Prenat Diagn 1998; 18: 1349-65.
  • 9Silber SJ, Nagy Z, Liu J, Tournaye H, Lissens W, Ferec C, etal.The use of epididymal and testicular spermatozoa for intracytoplasmic sperm injection: the genetic implications for male infertility. Hum Reprod 1995; 10:2031-43.
  • 10Eskenazi B, Wyrobek AJ, Kidd SA, Lowe X, Moore D 2nd,Weisiger K, et al. Sperm aneuploidy in fathers of children with paternally and maternally inherited Klinefelter syndrome. Hum Reprod 2002; 17:576-83.

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  • 1宋宁宏,吴宏飞,张炜,钱立新,苏建堂,周作民,沙家豪.特发性无精子症和严重少精子症患者无精子因子的检测及其意义[J].临床泌尿外科杂志,2005,20(4):213-215. 被引量:1
  • 2高雪峰,陈咏健,杨丽萍,李丹.常染色体异常与男性不育的细胞遗传学分析[J].中国优生与遗传杂志,2005,13(5):46-47. 被引量:19
  • 3郝丽君,崔英霞.1例罕见的AZFb部分缺失的少精子症[J].中华男科学杂志,2006,12(8):745-745. 被引量:8
  • 4Jin - Hu GUO, Pei - Yuan ZHU, Yu - Feng HUANG. Autosomal ab- errations associated with testicular dysgenesiso spermatogenic arrest in Chinese patients[J]. Androl,2002,4 ( 1 ) : 3 - 7.
  • 5王军荣,刘志婷,续微,关宝杰.45,XX,rob(13;14)染色体核型导致不孕及试管婴儿试验失败[J].中国妇幼保健,2007,22(33):4721-4722. 被引量:1
  • 6Li B, Li JB, Xiao XF, et al. Altered DNA methylation patterns of the H19 differentially methylated region and the DAZL gene promoter are assoeiated with defeetive human sperm. PLoS One, 2013, 8(8): e71215.
  • 7Teng YN, Lin YM, Lin YH, et al. Association of a single-nucleo- tide polymorphism of the deleted-in-azoospermia-like gene with susceptibility to spermatogenic failure. J Clin Endocrinol Metab, 2002, 87 ( 11 ) : 5258-5264.
  • 8Tschanter P, Kostova E, Luetjens CM, et al. No association of the A260G and A386G DAZL single nucleotide polymorphisms with male infertility in a Caucasian population. Hum Reprod, 2004, 19(12) : 2771-2776.
  • 9Reijo R, Lee TY, Salo P, et al. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat Genet, 1995, 10(4) : 383-393.
  • 10Xu EY, Moore FL, Pera RA. A gene family required for human germ cell development evolved from an ancient meiotic gene conserved in metazoans. Proc Natl Aead Sci U S A, 2001,98 (13) : 7414-7419.

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