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编码核呼吸因子1的人类基因的结构、表达及染色体定位

Structure, expression, and chromosomal assignment of the human gene encoding nuclear respiratory factor 1.

作者信息

Gopalakrishnan L, Scarpulla R C

机构信息

Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, Illinois 60611, USA.

出版信息

J Biol Chem. 1995 Jul 28;270(30):18019-25. doi: 10.1074/jbc.270.30.18019.

Abstract

Nuclear respiratory factor 1 (NRF-1) is a transcription factor that acts on nuclear genes encoding respiratory subunits and components of the mitochondrial transcription and replication machinery. Here we describe the isolation and characterization of the human gene encoding NRF-1. The human genomic sequences detected with NRF-1 cDNA probes at high stringency are all contained within seven overlapping recombinant lambda clones. The NRF-1 gene encompassed by these recombinants spans approximately 65 kilobases (kb) and has 11 exons and 10 introns that range in size from 0.8 to 15 kb. A rapid amplification of cDNA ends-polymerase chain reaction product containing the 5'-terminus of the NRF-1 cDNA has two exons from the 5'-untranslated region and terminates at a major transcription initiation site identified by S1 nuclease mapping. A genomic fragment containing a portion of the 5'-terminal exon and an additional 1 kb upstream had a functional promoter that was active in transfected COS cells, HeLa cells, and L6 myoblasts. The transcription initiation site utilized by the transfected promoter corresponded to that used by the endogenous gene in vivo. NRF-1 mRNA was expressed at very low levels in rat tissues compared with cytochrome c and, unlike cytochrome c, was most abundantly expressed in lung and testis. The NRF-1 gene was localized to human chromosome 7 by analysis of DNA from a panel of human-hamster cell hybrids with human-specific NRF-1 polymerase chain reaction primers. This assignment was further refined to 7q31 by cohybridization of NRF-1- and chromosome 7-specific probes to human metaphase chromosomes. These analyses should be useful in evaluating the potential role of NRF-1 in mitochondrial diseases resulting from defects in the nuclear control of mitochondrial function.

摘要

核呼吸因子1(NRF-1)是一种转录因子,作用于编码呼吸亚基以及线粒体转录和复制机制组成成分的核基因。在此,我们描述了编码NRF-1的人类基因的分离与特性分析。用NRF-1 cDNA探针在高严谨度条件下检测到的人类基因组序列全部包含在7个重叠的重组λ克隆中。这些重组体所包含的NRF-1基因跨度约为65千碱基(kb),有11个外显子和10个内含子,大小从0.8 kb到15 kb不等。包含NRF-1 cDNA 5'-末端的cDNA末端快速扩增-聚合酶链反应产物有来自5'-非翻译区的两个外显子,并在通过S1核酸酶作图确定的一个主要转录起始位点处终止。一个包含5'-末端外显子一部分及上游额外1 kb的基因组片段有一个功能性启动子,该启动子在转染的COS细胞、HeLa细胞和L6成肌细胞中具有活性。转染启动子所利用的转录起始位点与体内内源性基因所使用的位点相对应。与细胞色素c相比,NRF-1 mRNA在大鼠组织中的表达水平非常低,并且与细胞色素c不同,它在肺和睾丸中表达最为丰富。通过用人类特异性NRF-1聚合酶链反应引物分析一组人-仓鼠细胞杂种的DNA,将NRF-1基因定位到人类染色体7上。通过将NRF-1特异性探针和染色体7特异性探针与人类中期染色体进行共杂交,该定位进一步精确到7q31。这些分析对于评估NRF-1在因线粒体功能的核控制缺陷导致的线粒体疾病中的潜在作用应是有用的。

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