The Human Integrin β3 Gene Is 63 kb and Contains a 5′-UTR Sequence Regulating Expression

Author:

Wilhide Calvin C.1,Jin Ying1,Guo Qingbin1,Li Lu1,Li Su-Xia1,Rubin Edwin1,Bray Paul F.1

Affiliation:

1. From the Division of Hematology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD; and the Lawrence Berkeley Laboratories, Berkeley, CA.

Abstract

AbstractThe human blood platelet fibrinogen receptor, integrin αIIbβ3 (glycoprotein IIb-IIIa) is an archetypal member of the integrin family of adhesive molecules and is the only integrin encoded by genes physically linked in the genome. Because studies on the normal and abnormal expression of any gene require a thorough understanding of its organization, the initial goals of the current study were to determine the size and complete the genomic organization for the β3 gene. We now report the isolation of the entire β3 gene in a single P1 plasmid and for the first time have linked the first and second exons on a contiguous fragment of DNA. Using pulsed-field gel analysis, we determined the full size of the β3 gene to be 63 kb and show a large (16.7 kb) first intron; based on this information, we propose a uniform numbering system for the β3 exons. We have completed the 5′ genomic structure and generated a long-range restriction map. The promoter and the 5′ end of the first intron were found to have approximately 50% sequence identity with a region of the avian β3 gene known to possess functional transcriptional activity. Analysis of three different homologous regions led to the identification of a sequence in the 5′-UTR of the human gene, CCGCGGGAGG, which shares 90% identity with the avian gene and which bound nuclear proteins in DNaseI and electrophoretic mobility shift assay studies. Mutating this sequence caused a 2.6-fold reduction in reporter gene activity. In these studies we have (1) determined the full length and 5′ organization of the β3 gene, (2) identified a large region of homology between the 5′ regions of the avian and human genes, and (3) identified a sequence in the 5′-UTR that augments gene expression. Knowing the genomic structure of β3 has permitted the uncovering of new mechanisms of mutagenesis causing Glanzmann thrombasthenia (Jin et al, J Clin Invest 98:1745, 1996), and our findings will be valuable for such genetic analyses as well as for studies on the transcriptional regulation of β3 and other integrin genes.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference57 articles.

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