Azakie A, Larkin S B, Farrance I K, Grenningloh G, Ordahl C P
Department of Surgery, Cardiovascular Research Institute, University of California, San Francisco, 94143, USA. 674.
J Biol Chem. 1996 Apr 5;271(14):8260-5. doi: 10.1074/jbc.271.14.8260.
M-CAT motifs mediate muscle-specific transcriptional activity via interaction with binding factors that are antigenically and biochemically related to vertebrate transcription enhancer factor-1 (TEF-1), a member of the TEA/ATTS domain family of transcription factors. M-CAT binding activities present in cardiac and skeletal muscle tissues cannot be fully accounted for by existing cloned isoforms of TEF-1. TEF-1-related cDNAs isolated from heart libraries indicate that at least three classes of TEF-1-related cDNAs are expressed in these and other tissues. One class are homologues of the human TEF-1 originally cloned from HeLa cells (Xiao, J. H., Davidson, I., Matthes, H., Garnier, J. M., and Chambon, P. (1991) Cell 65, 551-568). A second class represents homologues of the avian TEF-1-related gene previously isolated (Stewart, A. F., Larkin, S. B., Farrance, I. K., Mar, J. H., Hall, D. E., and Ordahl, C. P. (1994) J. Biol. Chem. 269, 3147-3150). The third class consists of a novel, divergent TEF-1 cDNA, named DTEF-1, and its preliminary characterization is described here. Two isoforms of DTEF-1 (DTEF-1A and DTEF-1B) were isolated as 1.9-kilobase pair clones with putative open reading frames of 433 and 432 amino acids whose differences are attributable to alternative splicing at the C terminus of the TEA DNA binding domain. Cardiac muscle contains high levels of DTEF-1 transcripts, but unexpectedly low levels are detected in skeletal muscle. DTEF-1 transcripts are present at intermediate levels in gizzard and lung, and at low levels in kidney. DTEF-1A is a sequence-specific M-CAT-binding factor. The distinct spatial pattern of expression, and unusual amino acid sequence in its DNA binding domain, may indicate a particular role for DTEF-1 in cell-specific gene regulation. Recent work also suggests that at least one more TEF-1-related gene exists in vertebrates. We propose a naming system for the four TEF-1 gene family members identified to date that preserves existing nomenclature and provides a means for extending that nomenclature as additional family members may be identified.
M - CAT基序通过与一些结合因子相互作用来介导肌肉特异性转录活性,这些结合因子在抗原性和生化性质上与脊椎动物转录增强因子-1(TEF-1)相关,TEF-1是转录因子TEA/ATTS结构域家族的成员。心肌和骨骼肌组织中存在的M - CAT结合活性不能完全由现有的TEF-1克隆亚型来解释。从心脏文库中分离出的与TEF-1相关的cDNA表明,至少三类与TEF-1相关的cDNA在这些组织和其他组织中表达。一类是最初从HeLa细胞中克隆的人类TEF-1的同源物(肖,J.H.,戴维森,I.,马蒂斯,H.,加尼尔,J.M.,和尚邦,P.(1991年)《细胞》65卷,551 - 568页)。第二类代表先前分离出的禽类TEF-1相关基因的同源物(斯图尔特,A.F.,拉金,S.B.,法兰斯,I.K.,马尔,J.H.,霍尔,D.E.,和奥尔达尔,C.P.(1994年)《生物化学杂志》269卷,3147 - 3150页)。第三类由一个新的、不同的TEF-1 cDNA组成,命名为DTEF-1,本文描述了其初步特征。分离出DTEF-1的两种亚型(DTEF-1A和DTEF-1B),它们是1.9千碱基对的克隆,推测的开放阅读框分别为433和432个氨基酸,其差异归因于TEA DNA结合结构域C末端的可变剪接。心肌中含有高水平的DTEF-1转录本,但在骨骼肌中检测到的水平出乎意料地低。DTEF-1转录本在砂囊和肺中中等水平存在,在肾脏中低水平存在。DTEF-1A是一种序列特异性的M - CAT结合因子。其独特的表达空间模式及其DNA结合结构域中不寻常的氨基酸序列,可能表明DTEF-1在细胞特异性基因调控中具有特殊作用。最近的研究还表明,脊椎动物中至少还存在一个与TEF-1相关的基因。我们为迄今已鉴定的四个TEF-1基因家族成员提出了一个命名系统,该系统保留了现有的命名法,并为在可能鉴定出更多家族成员时扩展该命名法提供了一种方法。