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人类 Y 染色体的遗传学及其与男性不育的关联。

Genetics of the human Y chromosome and its association with male infertility.

机构信息

Department of Molecular and Cellular Biology, ICMR-National Institute for Research in Reproductive Health, JM Street, Parel, Mumbai, Maharashtra, 400012, India.

出版信息

Reprod Biol Endocrinol. 2018 Feb 17;16(1):14. doi: 10.1186/s12958-018-0330-5.

Abstract

The human Y chromosome harbors genes that are responsible for testis development and also for initiation and maintenance of spermatogenesis in adulthood. The long arm of the Y chromosome (Yq) contains many ampliconic and palindromic sequences making it predisposed to self-recombination during spermatogenesis and hence susceptible to intra-chromosomal deletions. Such deletions lead to copy number variation in genes of the Y chromosome resulting in male infertility. Three common Yq deletions that recur in infertile males are termed as AZF (Azoospermia Factor) microdeletions viz. AZFa, AZFb and AZFc. As estimated from data of nearly 40,000 Y chromosomes, the global prevalence of Yq microdeletions is 7.5% in infertile males; however the European infertile men are less susceptible to Yq microdeletions, the highest prevalence is in Americans and East Asian infertile men. In addition, partial deletions of the AZFc locus have been associated with infertility but the effect seems to be ethnicity dependent. Analysis of > 17,000 Y chromosomes from fertile and infertile men has revealed an association of gr/gr deletion with male infertility in Caucasians and Mongolian men, while the b2/b3 deletion is associated with male infertility in African and Dravidian men. Clinically, the screening for Yq microdeletions would aid the clinician in determining the cause of male infertility and decide a rational management strategy for the patient. As these deletions are transmitted to 100% of male offspring born through assisted reproduction, testing of Yq deletions will allow the couples to make an informed choice regarding the perpetuation of male infertility in future generations. With the emerging data on association of Yq deletions with testicular cancers and neuropsychiatric conditions long term follow-up data is urgently needed for infertile men harboring Yq deletions. If found so, the information will change the current the perspective of androgenetics from infertility and might have broad implication in men health.

摘要

人类 Y 染色体携带有负责睾丸发育以及成年后精子发生起始和维持的基因。Y 染色体的长臂(Yq)包含许多扩增和回文序列,使其在精子发生过程中容易发生自我重组,因此容易发生染色体内缺失。这种缺失导致 Y 染色体基因的拷贝数变异,导致男性不育。在不育男性中反复出现的三种常见 Yq 缺失被称为 AZF(无精子症因子)微缺失,即 AZFa、AZFb 和 AZFc。根据近 40000 条 Y 染色体的数据估计,全球不育男性 Yq 微缺失的患病率为 7.5%;然而,欧洲不育男性对 Yq 微缺失的敏感性较低,患病率最高的是美国和东亚不育男性。此外,AZFc 位点的部分缺失与不育有关,但这种效应似乎取决于种族。对来自生育能力正常和不育男性的>17000 条 Y 染色体的分析表明,在白种人和蒙古男性中,gr/gr 缺失与男性不育有关,而 b2/b3 缺失与非洲和德拉维达人男性的不育有关。临床上,Yq 微缺失的筛查将有助于临床医生确定男性不育的原因,并为患者制定合理的管理策略。由于这些缺失通过辅助生殖传递给 100%的男性后代,因此对 Yq 缺失的检测将使夫妇能够就未来几代男性不育的延续做出明智的选择。随着与 Yq 缺失相关的睾丸癌和神经精神疾病的相关数据的出现,迫切需要对携带 Yq 缺失的不育男性进行长期随访数据。如果发现了这种情况,这些信息将改变雄激素遗传学从不育症的当前观点,并可能对男性健康产生广泛影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ddf/5816366/811c0392835a/12958_2018_330_Fig1_HTML.jpg

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