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猪胞质苹果酸酶:cDNA克隆、测序及定位

Swine cytosolic malic enzyme: cDNA cloning, sequencing, and localization.

作者信息

Nunes M, Lahbib-Mansais Y, Geffrotin C, Yerle M, Vaiman M, Renard C

机构信息

Laboratoire mixte INRA-CEA de Radiobiologie appliquée, centre de recherche INRA de Jouy-en-Josas, 78352 France.

出版信息

Mamm Genome. 1996 Nov;7(11):815-21. doi: 10.1007/s003359900243.

Abstract

A highly significant genetic association has been found between some alleles of the swine Major Histocompatibility Complex SLA (Swine Leukocyte Antigen genetic complex) and the cytosolic malic enzymatic activity level in muscles. The aim of this study was to find out whether this genetic association was due to a close linkage of the SLA region and the gene coding for the enzyme. Since no swine cytosolic malic enzyme sequence (ME1) was available, we isolated several overlapping fragments that spanned the almost entire malic enzyme transcript both by screening of a swine cDNA library and by RT-PCR. The results indicated the existence of two transcripts of 2. 0 and 3.1 kb, which probably correspond to two alternative forms of one gene. The sequence of the transcript was highly similar to the other published mammalian cytosolic NADP+-dependent malic enzyme cDNA, especially within the four functional domains. Two major bands at 3.7 and 2.4 kb were detected on Northern blots containing the RNA from 25 tissues from fetuses and adult pigs. A high expression level was found in the adrenal gland, muscle, liver, and peripheral nerves. The analysis of malic enzyme RFLPs in five SLA informative families revealed an independent segregation of the ME1 gene from the SLA region. In situ hybridization results localized the cytosolic malic enzyme on the swine Chromosome (Chr) 1p1.2, except that the association between SLA and the malic enzyme activity level was due to a physical genetic linkage. Thus, the mechanisms underlying this association remain to be elucidated.

摘要

在猪主要组织相容性复合体SLA(猪白细胞抗原遗传复合体)的某些等位基因与肌肉中胞质苹果酸酶活性水平之间发现了高度显著的遗传关联。本研究的目的是确定这种遗传关联是否是由于SLA区域与编码该酶的基因紧密连锁所致。由于没有猪胞质苹果酸酶序列(ME1)可用,我们通过筛选猪cDNA文库和RT-PCR分离了几个重叠片段,这些片段几乎覆盖了整个苹果酸酶转录本。结果表明存在2.0和3.1 kb的两种转录本,它们可能对应于一个基因的两种可变形式。该转录本的序列与其他已发表的哺乳动物胞质NADP +依赖性苹果酸酶cDNA高度相似,尤其是在四个功能域内。在含有来自胎儿和成年猪25种组织的RNA的Northern印迹上检测到3.7和2.4 kb的两条主要条带。在肾上腺、肌肉、肝脏和外周神经中发现了高表达水平。对五个SLA信息丰富的家系中的苹果酸酶RFLP分析表明,ME1基因与SLA区域独立分离。原位杂交结果将胞质苹果酸酶定位在猪染色体(Chr)1p1.2上,除非SLA与苹果酸酶活性水平之间的关联是由于物理遗传连锁。因此,这种关联背后的机制仍有待阐明。

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