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肝脏mRNA探针揭示了两个与小鼠H-2S区域的补体C4基因座串联重复的细胞色素P-450基因。

Liver mRNA probes disclose two cytochrome P-450 genes duplicated in tandem with the complement C4 loci of the mouse H-2S region.

作者信息

Amor M, Tosi M, Duponchel C, Steinmetz M, Meo T

出版信息

Proc Natl Acad Sci U S A. 1985 Jul;82(13):4453-7. doi: 10.1073/pnas.82.13.4453.

Abstract

A search for uncharacterized genes of the S region of the murine H-2 major histocompatibility complex was undertaken; a series of cosmid clones previously aligned by overlap hybridizations were used as radiolabeled probes. Sequences hybridizing with liver poly(A)+ RNA were found within a cosmid covering a region 3' to the C4-Slp gene (the gene encoding the hemolytically inactive isoform of the fourth component of serum complement). Radiolabeled, short cDNA complementary to liver poly(A)+ RNA was used to establish the transcriptional polarity of the newly detected gene and to define fragments containing its 3' end. DNA sequence analyses and comparisons with porcine peptides established that the gene encodes the enzyme steroid 21-hydroxylase (EC 1.14.99.10), a cytochrome P-450 often referred to as P-450(C21), whose major site of expression is the adrenal gland. Two copies of the P-450(C21) gene, very similar yet distinguishable by restriction endonuclease analysis, were found individually associated with C4 and C4-Slp, genes that encode isoforms of mouse fourth component of complement. One of the P-450(C21) genes is coamplified with C4-Slp in H-2w7, a haplotype carrying a rare elongation of the S region. Comparisons with other members of the P-450 gene family show that the P-450(C21) genes encode peptides of extraordinary evolutionary conservation. The detection of a liver transcript of P-450(C21) raises the issue of the specific metabolic role of this enzyme in this organ and may have implications for the interpretation of human congenital adrenal hyperplasia.

摘要

对小鼠H-2主要组织相容性复合体S区未鉴定基因进行了搜索;一系列先前通过重叠杂交排列的黏粒克隆用作放射性标记探针。在一个覆盖C4-Slp基因(编码血清补体第四成分溶血无活性异构体的基因)3'端区域的黏粒中发现了与肝脏多聚腺苷酸加尾RNA(poly(A)+ RNA)杂交的序列。用与肝脏poly(A)+ RNA互补的放射性标记短cDNA来确定新检测到基因的转录极性,并确定包含其3'端的片段。DNA序列分析以及与猪肽的比较表明,该基因编码类固醇21-羟化酶(EC 1.14.99.10),一种通常称为P-450(C21)的细胞色素P-450,其主要表达位点是肾上腺。发现P-450(C21)基因的两个拷贝,它们非常相似但可通过限制性内切酶分析区分,分别与C4和C4-Slp相关联,C4和C4-Slp是编码小鼠补体第四成分异构体的基因。在H-2w7单倍型中,P-450(C21)基因之一与C4-Slp共同扩增,H-2w7单倍型的S区有罕见的延长。与P-450基因家族其他成员的比较表明,P-450(C21)基因编码具有非凡进化保守性的肽段。P-45(21)肝脏转录本的检测提出了该酶在该器官中具体代谢作用的问题,可能对人类先天性肾上腺增生的解释有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3297/391119/2027c58e6645/pnas00353-0161-a.jpg

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