Honoré B, Rasmussen H H, Vorum H, Dejgaard K, Liu X, Gromov P, Madsen P, Gesser B, Tommerup N, Celis J E
Danish Centre for Human Genome Research, Department of Medical Biochemistry, University of Aarhus, Denmark.
J Biol Chem. 1995 Dec 1;270(48):28780-9. doi: 10.1074/jbc.270.48.28780.
Molecular cDNA cloning, two-dimensional gel immunoblotting, and amino acid microsequencing identified three sequence-unique and distinct proteins that constitute a subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins corresponding to hnRNPs H, H', and F. These proteins share epitopes and sequence identity with two other proteins, isoelectric focusing sample spot numbers 2222 (37.6 kDa; pI 6.5) and 2326 (39.5 kDa; pI 6.6), indicating that the subfamily may contain additional members. The identity between hnRNPs H and H' is 96%, between H and F 78%, and between H' and F 75%, respectively. The three proteins contain three repeats, which we denote quasi-RRMs (qRRMs) since they have a remote similarity to the RNA recognition motif (RRM). The three qRRMs of hnRNP H, with a few additional NH2-terminal amino acids, were constructed by polymerase chain reaction amplification and used for ribohomopolymer binding studies. Each qRRM repeat bound poly(rG), while only the NH2-terminal qRRM bound poly(rC) and poly(rU). None of the repeats bound detectable amounts of poly(rA). The expression levels of hnRNPs H and F were differentially regulated in pairs of normal and transformed fibroblasts and keratinocytes. In normal human keratinocytes, the expression level of H was unaffected by treatment with several substances tested including two second messengers and seven cytokines. Likewise the expression level of F was independent of these substances, although it was strikingly down-regulated by long term treatment with 4 beta-phorbol 12-myristate 13-acetate, indicating that the protein kinase C signaling pathway regulates its expression. No effect of 4 beta-phorbol 12-myristate 13-acetate was observed on the expression of hnRNP H. The genes coding for hnRNPs H, H', and F were chromosome-mapped to 5q35.3 (HNRPH1), 6q25.3-q26, and/or Xq22 (HNRPH2) and 10q11.21-q11.22 (HNRPF), respectively.
分子cDNA克隆、二维凝胶免疫印迹和氨基酸微测序鉴定出三种序列独特且不同的蛋白质,它们构成了一个普遍表达的异质性核核糖核蛋白亚家族,分别对应于hnRNP H、H'和F。这些蛋白质与另外两种蛋白质(等电聚焦样品斑点编号2222,37.6 kDa;pI 6.5和2236,39.5 kDa;pI 6.6)共享表位和序列同一性,表明该亚家族可能包含其他成员。hnRNP H和H'之间的同一性为96%,H和F之间为78%,H'和F之间为75%。这三种蛋白质包含三个重复序列,我们将其称为准RNA识别基序(qRRMs),因为它们与RNA识别基序(RRM)有远缘相似性。通过聚合酶链反应扩增构建了hnRNP H的三个qRRMs,并添加了一些额外的NH2末端氨基酸,用于核糖同聚物结合研究。每个qRRM重复序列都能结合聚(rG),而只有NH2末端的qRRM能结合聚(rC)和聚(rU)。没有一个重复序列能结合可检测量的聚(rA)。hnRNP H和F的表达水平在正常和转化的成纤维细胞及角质形成细胞对中受到不同调节。在正常人角质形成细胞中,H的表达水平不受包括两种第二信使和七种细胞因子在内的几种测试物质处理的影响。同样,F的表达水平也与这些物质无关,尽管它在长期用4β-佛波醇12-肉豆蔻酸酯13-乙酸酯处理后显著下调,表明蛋白激酶C信号通路调节其表达。未观察到4β-佛波醇12-肉豆蔻酸酯13-乙酸酯对hnRNP H表达的影响。编码hnRNP H、H'和F的基因分别被染色体定位到5q35.3(HNRPH1)、6q25.3-q26和/或Xq22(HNRPH2)以及10q11.21-q11.22(HNRPF)。