Revised genomic organization of FBN1 and significance for regulated gene expression

被引:91
作者
Biery, NJ
Eldadah, ZA
Moore, CS
Stetten, G
Spencer, F
Dietz, HC
机构
[1] Johns Hopkins Univ, Sch Med, Inst Med Genet, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Obstet & Gynecol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
关键词
D O I
10.1006/geno.1998.5697
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
FBN1 encodes fibrillin-1, an extracellular matrix protein that is defective in Marfan syndrome, This gene is divided into 65 exons and was previously re ported to be approximately 110 kb in length. The existence of 3 exons upstream of the exon containing the putative initiating methionine left open the possibility of alternative fibrillin-1 isoforms that vary at their N-termini. Detailed examination of YACs containing human FBN1 reveal that the gene is 200 kb, almost twice as large as previously thought. Characterization of the porcine FBN1 cDNA and 5' flanking sequence demonstrates extreme conservation between the pig and the human predicted proteins and argues against the possibility of alternative amino-terminal coding sequence. These data further our understanding of the regulatory requirements for gene expression and establish a framework for recombinant expression of fibrillin-1. (C) 1999 Academic Press.
引用
收藏
页码:70 / 77
页数:8
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