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Alternatively spliced exons encode the tissue-specific 5' termini of leukocyte pp52 and stromal cell S37 mRNA isoforms.

作者信息

Thompson A A, Omori S A, Gilly M J, May W, Gordon M S, Wood W J, Miyoshi E, Malone C S, Gimble J, Denny C T, Wall R

机构信息

Department of Pediatrics, UCLA School of Medicine 90095, USA.

出版信息

Genomics. 1996 Mar 15;32(3):352-7. doi: 10.1006/geno.1996.0129.

DOI:10.1006/geno.1996.0129
PMID:8838798
Abstract

The pp52 gene encodes an intracellular, F-actin-binding phosphoprotein (also designated LSP1 and WP34) postulated to function in cytoskeleton dynamics and cell motility. We previously reported that different mRNA isoforms are expressed from this gene in cells of the leukocyte lineage versus mesodermally derived cells. These tissue-specific mRNA isoforms are identical except for 5'-untranslated regions and sequences coding for unique N-termini of 23 and 21 amino acids, respectively. As this is a single-copy gene, we predicted that these tissue-specific mRNA isoforms would be generated by alternative RNA splicing. We report that the unique 5' sequences in these mRNA isoforms are encoded in two separate exons containing ATG initiation codons. These features confirm that the pp52 and S37 mRNA isoforms are generated by alternative RNA splicing and establish that they are independently translated. Other results presented here indicate that the differential expression of these exons in leukocytes versus mesodermally derived cells is regulated at the level of transcription by tissue-specific promoters.

摘要

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