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鸡转录因子IIA的基因的染色体定位、结构、表达及需求

Chromosomal position, structure, expression, and requirement of genes for chicken transcription factor IIA.

作者信息

Mabuchi Tomoko, Wakamatsu Toshifumi, Nakadai Tomoyoshi, Shimada Miho, Yamada Kazuhiko, Matsuda Yoichi, Tamura Taka-Aki

机构信息

Department of Biology, Faculty of Science, Chiba University, Chiba, Japan.

出版信息

Gene. 2007 Aug 1;397(1-2):94-100. doi: 10.1016/j.gene.2007.04.015. Epub 2007 Apr 21.

DOI:10.1016/j.gene.2007.04.015
PMID:17544229
Abstract

Transcription factor IIA (TFIIA) is one of the general transcription factors for RNA polymerase II and composed of three subunits, TFIIAalpha, TFIIAbeta and TFIIAgamma. TFIIAalpha and TFIIAbeta are encoded by a single gene (TFIIAalphabeta) and mature through internal cleavage of TFIIAalphabeta. In this study, we found that structures of TFIIAalphabeta and TFIIAgamma are highly homologous with each mammalian counterpart. Exon-intron organizations of the human and chicken TFIIA genes were also homologous. The sequence of the cleavage region of the chicken TFIIAalphabeta precursor protein was fitted to the consensus cleavage recognition site. It was thus demonstrated that TFIIA is conserved in vertebrates. TFIIA proteins are present ubiquitously in chicken tissues. Fluorescent in situ hybridization revealed that TFIIAalphabeta and TFIIAgamma genes are located in chromosome 5 and a mini-chromosome, respectively. We generated semi-knockout chicken DT40 cells for TFIIAalphabeta and TFIIAgamma genes with high homologous recombination efficiencies, whereas we failed to establish double-knockout cells for each gene. It is thought that both genes for TFIIA are required in vertebrates. TFIIA siRNA resulted in deceleration of cell growth rate, suggesting that, consistent with those of knockout assays, TFIIA is associated with cell growth regulation.

摘要

转录因子IIA(TFIIA)是RNA聚合酶II的通用转录因子之一,由三个亚基组成,即TFIIAα、TFIIAβ和TFIIAγ。TFIIAα和TFIIAβ由单个基因(TFIIAαβ)编码,并通过TFIIAαβ的内部切割而成熟。在本研究中,我们发现TFIIAαβ和TFIIAγ的结构与每个哺乳动物对应物高度同源。人和鸡TFIIA基因的外显子-内含子组织也具有同源性。鸡TFIIAαβ前体蛋白的切割区域序列符合共有切割识别位点。因此证明TFIIA在脊椎动物中是保守的。TFIIA蛋白在鸡组织中普遍存在。荧光原位杂交显示TFIIAαβ和TFIIAγ基因分别位于5号染色体和一条小染色体上。我们以高同源重组效率生成了TFIIAαβ和TFIIAγ基因的半敲除鸡DT40细胞,然而我们未能建立每个基因的双敲除细胞。据认为,TFIIA的这两个基因在脊椎动物中都是必需的。TFIIA siRNA导致细胞生长速率减慢,这表明,与敲除试验的结果一致,TFIIA与细胞生长调节有关。

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