Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/9959
Title: Tissue-specific and allelic expression of the complement regulator CD46 is controlled by alternative splicing.
Authors: Russell, S M;Sparrow, R L;McKenzie, Ian F C;Purcell, D F
Affiliation: Austin Research Institute, Austin Hospital, Heidelberg, Victoria, Australia.
Issue Date: 1-Jun-1992
Citation: European Journal of Immunology; 22(6): 1513-8
Abstract: CD46 (membrane cofactor protein) is a human cell surface glycoprotein with cofactor activity for factor I-mediated cleavage of complement components C3b and C4b. The CD46 protein from normal lymphocytes resolves on sodium dodecyl sulfate-polyacrylamide gel electrophoresis as two major bands of 66 and 56 kDa. CD46 cDNA encodes four extracellular short consensus repeat domains, a Ser/Thr/Pro (STP)-rich region, a transmembrane region and a cytoplasmic tail. We now show that exquisite control of mRNA splicing is responsible for the heterogeneous expression of CD46 isoforms. Differential splicing of 5 exons generates at least 14 CD46 mRNA variants whose expression is stringently regulated by allelic, tissue-specific and malignancy-related factors, as: (a) leukemic cells and Epstein-Barr virus-transformed B cells preferentially incorporate the first of three STP exons (exon 7) into mRNA, and produce a larger CD46 isoform of 74 kDa, (b) an allelic difference in the proportion of 66- and 56-kDa CD46 isoforms on lymphocytes corresponds to the preferential inclusion or exclusion of the second STP exon (exon 8), (c) the third STP exon (exon 9) is specifically deleted in some placentae, (d) spermatozoa delete both exons 12 and 13, encoding a shorter transmembrane region and a unique cytoplasmic tail and (e) all tissues tested differentially splice exon 13, resulting in two alternative cytoplasmic tails. The distribution of the 14 alternatively spliced RNA transcripts correlated with the presence of protein isoforms of the predicted size, indicating that alternative splicing leads to heterogeneity of CD46 glycoproteins.
Internal ID Number: 1601037
URI: http://ahro.austin.org.au/austinjspui/handle/1/9959
DOI: 10.1002/eji.1830220625
URL: http://www.ncbi.nlm.nih.gov/pubmed/1601037
Type: Journal Article
Subjects: Alleles
Amino Acid Sequence
Antigens, CD.biosynthesis
Antigens, CD46
Base Sequence
Blotting, Western
Chromosome Mapping
Colonic Neoplasms.immunology
Exons
Gene Expression Regulation.genetics
Granulocytes.immunology
Humans
Isoantigens.biosynthesis
Leukemia.immunology
Lymphocytes.immunology
Male
Membrane Glycoproteins.biosynthesis
Molecular Sequence Data
Organ Specificity
Placenta.immunology
Polymerase Chain Reaction
RNA Splicing.physiology
Sequence Homology, Nucleic Acid
Spermatozoa.immunology
Transcription, Genetic
Appears in Collections:Journal articles

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