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人类载脂蛋白B基因定位于2号染色体短臂,并证实存在双等位基因限制性片段长度多态性。

Mapping of the human APOB gene to chromosome 2p and demonstration of a two-allele restriction fragment length polymorphism.

作者信息

Huang L S, Miller D A, Bruns G A, Breslow J L

出版信息

Proc Natl Acad Sci U S A. 1986 Feb;83(3):644-8. doi: 10.1073/pnas.83.3.644.

Abstract

ApoB is a large glycoprotein with an apparent molecular mass of 550 kDa on NaDodSO4/PAGE. It is a major constituent of most lipoproteins and plays an important role in their metabolism. Recently, apoB cDNA clones have been isolated from an expression library made with mRNA from a human hepatoma cell line. These clones, which were all 1.5-1.6 kilobases (kb) long and corresponded to the 3' end of apoB mRNA, were used to demonstrate that hepatic apoB mRNA is approximately 22 kb long. In the current report, a probe derived from one of these cDNA clones, pB8, was used for in situ hybridization experiments to map the human gene for apoB, APOB, to the distal half of the short arm of chromosome 2. This probe was also used to analyze somatic cell hybrids and, in agreement with the in situ hybridization studies, concordancy was demonstrated with chromosome 2. In addition, two hybrids with chromosome 2 translocations that contain only the short arm reacted with the pB8 probe. A third hybrid with a complex rearrangement of chromosome 2, which deleted an interstitial region and the tip of the short arm of chromosome 2, did not react. These data indicate that APOB maps to either 2p21-p23 or 2p24-pter. In further studies, DNA from normal individuals, digested with the restriction endonuclease EcoRI and subjected to Southern blot analysis with the pB8 probe, revealed a two-allele restriction fragment length polymorphism (RFLP). The major allele was 11 kb, and the minor allele was 13 kb. The minor allele was present with a frequency of 20-25%. The inheritance of the two alleles was studied in an informative family, and they segregated in a typical autosomal Mendelian fashion. The mapping studies provide the means for understanding the relationship of the APOB locus to others in the human genome, whereas the demonstration of an APOB RFLP increases our ability to assess the role of this locus in determining plasma lipoprotein levels.

摘要

载脂蛋白B(ApoB)是一种大型糖蛋白,在十二烷基硫酸钠聚丙烯酰胺凝胶电泳(NaDodSO4/PAGE)上的表观分子量为550 kDa。它是大多数脂蛋白的主要成分,在其代谢中起重要作用。最近,已从用人肝癌细胞系的mRNA构建的表达文库中分离出载脂蛋白B cDNA克隆。这些克隆长度均为1.5 - 1.6千碱基(kb),对应于载脂蛋白B mRNA的3'端,用于证明肝脏载脂蛋白B mRNA约为22 kb长。在本报告中,源自这些cDNA克隆之一pB8的探针用于原位杂交实验,将人类载脂蛋白B基因(APOB)定位到2号染色体短臂的远端一半。该探针还用于分析体细胞杂种,与原位杂交研究一致,显示与2号染色体相符。此外,两个含有仅2号染色体短臂的2号染色体易位杂种与pB8探针发生反应。第三个具有2号染色体复杂重排的杂种,其缺失了2号染色体短臂的中间区域和末端,未发生反应。这些数据表明APOB定位于2p21 - p23或2p24 - 末端。在进一步研究中,用限制性内切酶EcoRI消化正常个体的DNA,并用pB8探针进行Southern印迹分析,揭示了一种双等位基因限制性片段长度多态性(RFLP)。主要等位基因为11 kb,次要等位基因为13 kb。次要等位基因的频率为20% - 25%。在一个信息丰富的家系中研究了这两个等位基因的遗传,它们以典型的常染色体孟德尔方式分离。定位研究为理解APOB基因座与人类基因组中其他基因座的关系提供了手段,而APOB RFLP的证明增强了我们评估该基因座在决定血浆脂蛋白水平中作用的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b19a/322920/a7ea5531b6b1/pnas00307-0126-a.jpg

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