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人类ZHX1:克隆、染色体定位及其与转录因子NF-Y的相互作用。

Human ZHX1: cloning, chromosomal location, and interaction with transcription factor NF-Y.

作者信息

Yamada K, Printz R L, Osawa H, Granner D K

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, 707 Light Hall, Nashville, Tennessee, 37232-0615, USA.

出版信息

Biochem Biophys Res Commun. 1999 Aug 11;261(3):614-21. doi: 10.1006/bbrc.1999.1087.

Abstract

NF-YA, B, and C comprise the heterotrimeric transcription factor known as nuclear factor Y (NF-Y) or CCAAT-binding protein (CBF). NF-Y binds many CCAAT and Y box (an inverted CCAAT box, ATTGG) elements. Mutations of these elements that disrupt the binding of NF-Y result in decreased transcription from various tissue-specific and inducible promoters. We employed a yeast two-hybrid system to screen a human liver cDNA library in an effort to isolate proteins that interact with NF-Y and that may play a role in tissue-specific or hormone-inducible promoter activity. Using a fragment of the NF-YA subunit as bait we isolated a cDNA that encodes most of the open reading frame of the human zinc fingers and homeobox 1 (ZHX1) protein. The complete open reading frame was subsequently isolated and found to encode a protein of 873 amino acids that contains two zinc fingers and five homeodomain motifs. Northern blot analysis of poly(A)(+) RNA isolated from various tissues revealed two major ZHX1 transcripts of about 4.5 and 5 kilobases. Both transcripts were expressed ubiquitously, although the 5-kilobase transcript is of greater abundance in most tissues examined. The human ZHX1 gene is located on chromosome 8q, between markers CHCL.GATA50B06 and CHLC. GATA7G07.

摘要

NF-YA、NF-YB和NF-YC组成了被称为核因子Y(NF-Y)或CCAAT结合蛋白(CBF)的异源三聚体转录因子。NF-Y能结合许多CCAAT元件和Y盒(一种反向CCAAT盒,ATTGG)。这些元件发生突变从而破坏NF-Y的结合,会导致各种组织特异性启动子和诱导型启动子的转录减少。我们利用酵母双杂交系统筛选人肝脏cDNA文库,以分离与NF-Y相互作用且可能在组织特异性或激素诱导型启动子活性中发挥作用的蛋白质。以NF-YA亚基的一个片段作为诱饵,我们分离出了一个cDNA,它编码人锌指和同源框1(ZHX1)蛋白的大部分开放阅读框。随后分离出了完整的开放阅读框,发现它编码一个含有873个氨基酸的蛋白质,该蛋白质包含两个锌指和五个同源结构域基序。对从各种组织中分离出的聚腺苷酸(poly(A))RNA进行Northern印迹分析,发现了两种主要的ZHX1转录本,大小约为4.5和5千碱基。两种转录本均在各处表达,不过在大多数检测的组织中,5千碱基的转录本丰度更高。人ZHX1基因位于8号染色体q上,在标记CHCL.GATA50B06和CHLC.GATA7G07之间。

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