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编码单倍体生殖细胞特异性核蛋白激酶的人类Haspin基因的克隆与特性分析。

Cloning and characterization of human haspin gene encoding haploid germ cell-specific nuclear protein kinase.

作者信息

Tanaka H, Iguchi N, Nakamura Y, Kohroki J, de Carvalho C E, Nishimune Y

机构信息

Department of Science for Laboratory Animal Experimentation, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita City, Osaka 565-0871, Japan.

出版信息

Mol Hum Reprod. 2001 Mar;7(3):211-8. doi: 10.1093/molehr/7.3.211.

Abstract

We report here the molecular cloning and characterization of human haspin cDNA and its genomic DNA construct. The haspin protein is a unique protein kinase, first isolated from mouse testis. Specifically expressed in mouse testicular germ cells, haspin is suggested to play a role in cell cycle arrest in haploid spermatids. Detection of human haspin by Northern blot analysis showed that the major transcript was 2.8 kilobases long and detected exclusively in the testis. The entire coding region of the human cDNA showed 68% identity with mouse haspin. The predicted amino acid sequence showed strong conservation of the kinase catalytic domain, leucine zipper, potential phosphorylation sites, and MEF2B homologous region, but a relatively unique N:-terminal region. Human haspin protein was also demonstrated to have protein kinase activity. The human haspin gene was mapped to chromosome 17p13 by computer database cloning of human genomic DNA. Furthermore, the genomic structure of human haspin was proven to be intronless and the whole transcription unit was found to be located in an intron of the integrin alphaE2 gene.

摘要

我们在此报告人Haspin cDNA及其基因组DNA构建体的分子克隆和特性分析。Haspin蛋白是一种独特的蛋白激酶,最初从小鼠睾丸中分离得到。Haspin在小鼠睾丸生殖细胞中特异性表达,提示其在单倍体精子细胞的细胞周期停滞中发挥作用。通过Northern印迹分析检测人Haspin,结果显示主要转录本长2.8千碱基,且仅在睾丸中检测到。人cDNA的整个编码区与小鼠Haspin有68%的同一性。预测的氨基酸序列显示激酶催化结构域、亮氨酸拉链、潜在磷酸化位点和MEF2B同源区域具有高度保守性,但N端区域相对独特。人Haspin蛋白也被证明具有蛋白激酶活性。通过对人基因组DNA进行计算机数据库克隆,将人Haspin基因定位到染色体17p13。此外,已证实人Haspin的基因组结构无内含子,且整个转录单元位于整合素αE2基因的一个内含子中。

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