Farmer A A, Loftus T M, Mills A A, Sato K Y, Neill J D, Tron T, Yang M, Trumpower B L, Stanbridge E J
Department of Microbiology and Molecular Genetics, University of California Irvine, College of Medicine 92715.
Hum Mol Genet. 1994 May;3(5):723-8. doi: 10.1093/hmg/3.5.723.
QM is a 214 amino acid polypeptide, encoded by a gene (DXS648) in Xq28, that contains a high percentage of charged amino acids and has been found to bind c-Jun and DNA. Searches of the GenBank database revealed no matches between QM and any other known transcription factors. However, we and others have isolated QM homologs from a diverse array of eukaryotes. Alignment of these sequences indicated a high degree of conservation throughout the first 175 residues of the protein and revealed several interesting features. Most notable is the considerable conservation of charged amino acids within specific regions of the protein. Secondary structure analysis suggests that two of these regions form amphipathic alpha-helices, one basic and one acidic. A third conserved charged domain, comprising the N-terminal 30 amino acids, is both basic and proline rich. The rate of sequence divergence of the various homologs was found to be slow (of the order of 1% change every 22 million years), consistent with a critical role for QM in eukaryotic cells. A role for QM as a novel class of transcription regulatory protein is suggested.
QM是一种由位于Xq28的基因(DXS648)编码的214个氨基酸的多肽,该多肽含有高比例的带电荷氨基酸,并且已被发现能结合c-Jun和DNA。对GenBank数据库的搜索显示,QM与任何其他已知转录因子均不匹配。然而,我们和其他人已从多种真核生物中分离出QM同源物。这些序列的比对表明,该蛋白质的前175个残基具有高度保守性,并揭示了几个有趣的特征。最值得注意的是该蛋白质特定区域内带电荷氨基酸的显著保守性。二级结构分析表明,其中两个区域形成两亲性α螺旋,一个呈碱性,一个呈酸性。第三个保守的带电荷结构域,由N端的30个氨基酸组成,既呈碱性又富含脯氨酸。发现各种同源物的序列分歧率较慢(每2200万年变化约1%),这与QM在真核细胞中的关键作用一致。有人提出QM作为一类新型转录调节蛋白发挥作用。