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HSFY的特征分析,Y染色体上一个新的AZFb基因,可能在人类精子发生中发挥作用。

Characterization of HSFY, a novel AZFb gene on the Y chromosome with a possible role in human spermatogenesis.

作者信息

Tessari A, Salata E, Ferlin A, Bartoloni L, Slongo M L, Foresta C

机构信息

Department of Medical and Surgical Sciences, Centre for Male Gamete Cryopreservation, University of Padua, Via Ospedale 105, 35128 Padua, Italy.

出版信息

Mol Hum Reprod. 2004 Apr;10(4):253-8. doi: 10.1093/molehr/gah036. Epub 2004 Feb 16.

Abstract

HSFY (heat shock transcription factor, Y chromosome) has been mapped in the AZFb region of the Y chromosome, whose deletion results in severe male infertility. HSFY belongs to the heat shock factor family that has been shown to be implicated in spermatogenesis both in animals and humans. We report the characterization of the genomic structure, the number of copies on the Y chromosome and the expression of the gene. By comparison of data obtained from expression analysis and from GenBank cDNA sequences, seven exons were identified. Alternative splicing generates three different transcripts and proteins, each containing an HSF domain typical of HSF proteins. Two identical and functional full-length copies of HSFY map in palindrome P4 of AZFb, whereas four similar sequences mapping in two clusters in palindrome P1 of AZFc and P3 seem to represent pseudogenes. Sequences similar to few HSFY exons are also located in the short arm of chromosomes Y, X and 22. Expression analysis revealed that the three HSFY transcripts are differentially expressed, transcript 1 being present in many tissues including testis and ejaculated sperm, and transcripts 2 and 3 being testis-specific. These data suggest that HSFY could have an important role in human spermatogenesis.

摘要

热休克转录因子Y染色体相关基因(HSFY)已被定位在Y染色体的无精子因子b(AZFb)区域,该区域的缺失会导致严重的男性不育。HSFY属于热休克因子家族,已证明该家族在动物和人类的精子发生过程中均有涉及。我们报告了该基因的基因组结构特征、Y染色体上的拷贝数以及基因表达情况。通过比较表达分析数据和GenBank cDNA序列,确定了7个外显子。可变剪接产生了三种不同的转录本和蛋白质,每种都含有热休克因子(HSF)蛋白特有的HSF结构域。两个相同且具有功能的全长HSFY拷贝定位于AZFb的回文序列P4中,而在AZFc的回文序列P1和P3中的两个簇中定位的四个相似序列似乎代表假基因。与少数HSFY外显子相似的序列也位于Y、X和22号染色体的短臂上。表达分析表明,三种HSFY转录本的表达存在差异,转录本1存在于包括睾丸和射出精子在内的许多组织中,而转录本2和3则是睾丸特异性的。这些数据表明,HSFY可能在人类精子发生过程中发挥重要作用。

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