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人类BACH1转录调节基因的分离,该基因定位于21号染色体的22.1区带。

Isolation of the human BACH1 transcription regulator gene, which maps to chromosome 21q22.1.

作者信息

Blouin J L, Duriaux Saïl G, Guipponi M, Rossier C, Pappasavas M P, Antonarakis S E

机构信息

Division of Medical Genetics, Centre Médical Universitaire, Genève, Switzerland.

出版信息

Hum Genet. 1998 Mar;102(3):282-8. doi: 10.1007/s004390050692.

Abstract

In order to contribute to the development of the transcriptional map of chromosome 21, we performed exon trapping using cosmid clones mapped in the region 21q22.1-22.2 and identified a number of potential exons. One of the trapped exons (Genbank No. AF026200) showed a strong homology with the mouse Bach1 gene (Genbank No. D86603), a transcription factor regulating gene expression. We then isolated the full-length coding region of the human BACH1 gene using expressed sequence tags, reverse transcription-polymerase chain reaction and rapid amplification of cDNA ends. The predicted BACH1 protein contains 736 amino acids and is 88% identical to its mouse homolog. It contains basic leucine zipper and BTB-zinc finger domains (which are directly involved in DNA binding for transcription regulation). The BACH1 gene maps in a relatively gene-poor region on 21q22.1 in yeast artificial chromosome 814c1 of the collection of Chumakov et al. Northern blot analysis revealed that it is expressed as an mRNA species of approximately 5.8 kb in all 16 adult and 4 fetal tissues examined; an additional mRNA species of 2.8 kb was observed in adult testis. The contribution of the BACH1 gene to the pathophysiology of trisomy or monosomy 21 is unknown. In addition, no monogenic disorders associated with mutations in the BACH1 gene have yet been identified.

摘要

为了推动21号染色体转录图谱的发展,我们使用定位在21q22.1 - 22.2区域的黏粒克隆进行外显子捕获,并鉴定出了一些潜在外显子。其中一个捕获的外显子(Genbank编号:AF026200)与小鼠Bach1基因(Genbank编号:D86603)具有高度同源性,后者是一种调节基因表达的转录因子。随后,我们利用表达序列标签、逆转录 - 聚合酶链反应以及cDNA末端快速扩增技术,分离出了人类BACH1基因的全长编码区。预测的BACH1蛋白包含736个氨基酸,与小鼠同源蛋白的一致性为88%。它含有碱性亮氨酸拉链和BTB - 锌指结构域(直接参与转录调控的DNA结合)。BACH1基因定位在Chumakov等人收集的酵母人工染色体814c1中21q22.1上一个基因相对较少的区域。Northern印迹分析显示,在所检测的16种成人组织和4种胎儿组织中,它均表达为一种约5.8 kb的mRNA;在成人睾丸中还观察到一种2.8 kb的额外mRNA。BACH1基因对21三体或21单体病理生理学的贡献尚不清楚。此外,尚未鉴定出与BACH1基因突变相关的单基因疾病。

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