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日本男性中编码精子发生特异性肌动蛋白样蛋白的无内含子ACTL7A和ACTL7B基因内的遗传多态性

Genetic Polymorphisms within The Intronless ACTL7A and ACTL7B Genes Encoding Spermatogenesis-Specific Actin-Like Proteins in Japanese Males.

作者信息

Tanaka Hiromitsu, Miyagawa Yasushi, Tsujimura Akira, Wada Morimasa

机构信息

Faculty of Pharmaceutical Sciences, Nagasaki International University, Huis Ten Bosch, Sasebo, Nagasaki, Japan.Electronic Address:

Department of Urology, Graduate School of Medicine, Osaka University, Yamadaoka, Suita, Osaka, Japan.

出版信息

Int J Fertil Steril. 2019 Oct;13(3):245-249. doi: 10.22074/ijfs.2019.5702. Epub 2019 Jul 14.

Abstract

Actins play essential roles in cellular morphogenesis. In mice, the and 2 genes, which encode actin-like proteins, are specifically expressed in haploid germ cells. Both and have also been cloned and studied. The orthologous genes in humans are present on chromosome 9q31.3 as intronless genes. Defects of germ cell-specific genes can introduce infertility without somatic function impairment. We determined T-ACTIN1 and 2, specifically expressed in the testis using reverse-transcription polymerase chain reaction (RT-PCR). To examine whether genetic polymorphisms of the and 2 genes are associated with male infertility, we screened for and 2 polymorphisms by direct sequencing of DNA from 282 sterile and 89 fertile Japanese men. We identified five and six single nucleotide polymorphisms (SNPs) in the and 2 regions of the sterile and fertile subjects respectively. Among these genetic polymorphisms was a novel SNP that was not in the National Center for Biotechnology Information SNP database. Although we could not determine whether these SNPs cause infertility, the prevalence of these genetic polymorphisms may be useful for analyzing polymorphisms in future largescale genetic analyses.

摘要

肌动蛋白在细胞形态发生中发挥着重要作用。在小鼠中,编码肌动蛋白样蛋白的 和 2 基因在单倍体生殖细胞中特异性表达。 和 也已被克隆和研究。人类中的同源基因作为无内含子基因存在于9号染色体的31.3区。生殖细胞特异性基因的缺陷可导致不育,而不损害体细胞功能。我们使用逆转录聚合酶链反应(RT-PCR)确定了在睾丸中特异性表达的T-ACTIN1和2。为了研究 和 2 基因的遗传多态性是否与男性不育有关,我们通过直接测序282名不育和89名生育能力正常的日本男性的DNA来筛选 和 2 的多态性。我们在不育和生育能力正常的受试者的 和 2 区域分别鉴定出5个和6个单核苷酸多态性(SNP)。在这些遗传多态性中,有一个新的SNP不在美国国立生物技术信息中心的SNP数据库中。虽然我们无法确定这些SNP是否导致不育,但这些遗传多态性的发生率可能有助于未来大规模遗传分析中的多态性分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dc2/6642428/32b7d85c812c/Int-J-Fertil-Steril-13-245-g01.jpg

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