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人血小板因子4和PF4alt基因的结构与功能比较

Structural and functional comparison of the genes for human platelet factor 4 and PF4alt.

作者信息

Eisman R, Surrey S, Ramachandran B, Schwartz E, Poncz M

机构信息

Division of Hematology, Children's Hospital of Philadelphia, PA 19104.

出版信息

Blood. 1990 Jul 15;76(2):336-44.

PMID:1695112
Abstract

Platelet factor 4 (PF4) is a 70 amino acid heparin-binding protein released from the alpha-granules of activated platelets. Its exact biologic function is not known, although PF4 is a member of a multigene family involved in chemotaxis, coagulation, inflammation, and cell growth. We previously cloned the cDNA for human PF4 from a human erythroleukemic (HEL) cell expression library. We now report the isolation and sequence determination of the gene for human PF4. This gene contains three exons and spans approximately 1,000 basepairs (bp). Concurrently, we have cloned a highly homologous gene that we have called PF4alt. We show that PF4 and PF4alt are non-allelic genes: the human PF4 gene is encoded on a 10 kilobasepairs (kb) EcoRI fragment, and its DNA sequence agrees with protein and cDNA data for PF4, while PF4alt is encoded in a polymorphic 3 or 5 kb EcoRI fragment. Compared with PF4, this gene has 14% DNA and 38% amino acid divergence in the signal peptide region, and 2.6% DNA and 4.3% amino acid divergence in the coding region of the mature protein. PF4alt contains three amino acid substitutions (P58----L, K66----E, and L67----H) near the C-terminus, in a region known to be critical for PF4 function. Primer extension studies show the 5'-untranslated region of PF4 is 73 bp long. A TATA box is present 30 bp 5' to the transcription start site. A 90 bp stretch of pyrimidines (including 53 consecutive thymidine residues) begins at -227 bp and is analogous to a similar region of 30 residues 5' to the rodent PF4 gene. This pyrimidine-rich region is absent from the PF4alt gene; however, DNA homology exists between the two human genes in the 5'- and 3'-flanking regions and extends for over 3.6 kb. Alternating purine/pyrimidine tracts occur both 5' and 3' to PF4 and PF4alt but do not define the endpoints of the gene duplication, which extend beyond these sequences at least at the 5' end. Northern blot analysis using gene-specific oligonucleotides and platelet RNA showed an 800 or 900 nucleotide (n) message for PF4 and PF4alt, respectively. Northern blot and primer extension studies show that steady-state platelet PF4 mRNA levels are approximately one magnitude greater than PF4alt mRNA levels. Thus, these studies demonstrate that PF4alt mRNA is expressed in platelets. Whether PF4alt protein is expressed remains to be determined, and the nature of its biologic function needs to be studied.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

血小板因子4(PF4)是一种由活化血小板的α-颗粒释放的含70个氨基酸的肝素结合蛋白。尽管PF4是参与趋化作用、凝血、炎症和细胞生长的多基因家族成员,但其确切生物学功能尚不清楚。我们之前从人红白血病(HEL)细胞表达文库中克隆了人PF4的cDNA。我们现在报告人PF4基因的分离和序列测定。该基因包含三个外显子,跨度约为1000个碱基对(bp)。同时,我们克隆了一个高度同源的基因,我们将其命名为PF4alt。我们表明PF4和PF4alt是非等位基因:人PF4基因编码在一个10千碱基对(kb)的EcoRI片段上,其DNA序列与PF4的蛋白质和cDNA数据一致,而PF4alt编码在一个多态性的3或5 kb EcoRI片段中。与PF4相比,该基因在信号肽区域有14%的DNA差异和38%的氨基酸差异,在成熟蛋白的编码区域有2.6%的DNA差异和4.3%的氨基酸差异。PF4alt在靠近C端的区域含有三个氨基酸取代(P58→L、K66→E和L67→H),该区域已知对PF4功能至关重要。引物延伸研究表明PF4的5'-非翻译区长度为73 bp。在转录起始位点上游30 bp处存在一个TATA框。一段90 bp的嘧啶序列(包括53个连续的胸腺嘧啶残基)从-227 bp处开始,类似于啮齿动物PF4基因5'端的一个30个残基的类似区域。PF4alt基因中不存在这个富含嘧啶的区域;然而,这两个人类基因在5'-和3'-侧翼区域存在DNA同源性,并且延伸超过3.6 kb。嘌呤/嘧啶交替序列出现在PF4和PF4alt的5'和3'端,但并未界定基因重复的端点,基因重复至少在5'端超出了这些序列。使用基因特异性寡核苷酸和血小板RNA进行的Northern印迹分析显示,PF4和PF4alt分别有一个800或900核苷酸(n)的信使RNA。Northern印迹和引物延伸研究表明,稳态血小板PF4 mRNA水平比PF4alt mRNA水平大约高一个数量级。因此,这些研究表明PF4alt mRNA在血小板中表达。PF4alt蛋白是否表达还有待确定,其生物学功能的性质也需要研究。(摘要截短至400字)

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