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从HeLa细胞中分离并鉴定出两个新的、密切相关的ATF cDNA克隆。

Isolation and characterization of two novel, closely related ATF cDNA clones from HeLa cells.

作者信息

Gaire M, Chatton B, Kedinger C

机构信息

Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire, Strasbourg, France.

出版信息

Nucleic Acids Res. 1990 Jun 25;18(12):3467-73. doi: 10.1093/nar/18.12.3467.

Abstract

ATF or CRE binding proteins are cellular transcription factors involved in the regulation of adenovirus Ela-responsive and cellular cAMP-inducible promoters. We report the isolation from a HeLa cell cDNA library of two clones that encode proteins with specific ATF/CRE DNA binding activity. The two clones differ by a 63 bp element which is retained in one (ATF-a) and deleted from the other (ATF-a delta) and which may correspond to an alternative exon. The peptide sequences (483 and 462 amino acids, respectively) derived from each of these cDNAs are identical, except for the additional 21 amino acids in ATF-a, but clearly differ from the other ATF/CREB proteins reported. All of them, however, share a conserved leucine zipper domain also found in other transcription factors. ATF-a and ATF-a delta therefore represent two closely related members of a larger multigene family of proteins that interact with conserved promoter elements.

摘要

ATF或CRE结合蛋白是参与腺病毒E1a反应性和细胞cAMP诱导性启动子调控的细胞转录因子。我们报道了从HeLa细胞cDNA文库中分离出两个克隆,它们编码具有特定ATF/CRE DNA结合活性的蛋白质。这两个克隆的差异在于一个63bp的元件,该元件在一个克隆(ATF-α)中保留,而在另一个克隆(ATF-αδ)中缺失,并且可能对应于一个可变外显子。分别从这些cDNA推导的肽序列(分别为483和462个氨基酸)除了ATF-α中额外的21个氨基酸外是相同的,但明显不同于已报道的其他ATF/CREB蛋白。然而,它们都共享一个在其他转录因子中也发现的保守亮氨酸拉链结构域。因此,ATF-α和ATF-αδ代表了与保守启动子元件相互作用的更大的多基因家族蛋白质中两个密切相关的成员。

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