Evolution of Transglutaminase Genes: Identification of a Transglutaminase Gene Cluster on Human Chromosome 15q15
We isolated and characterized the gene encoding human transglutaminase (TG)X(TGM5) and mapped it to the 15q15.2 region of chromosome 15 by fluorescence in situ hybridization. The gene consists of 13 exons separated by 12 introns and spans about 35 kilobases. Further sequence analysis and mapping sho...
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Published in | The Journal of biological chemistry Vol. 276; no. 35; pp. 33066 - 33078 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.08.2001
American Society for Biochemistry and Molecular Biology |
Online Access | Get full text |
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Summary: | We isolated and characterized the gene encoding human transglutaminase (TG)X(TGM5) and mapped it to the 15q15.2 region of chromosome 15 by fluorescence in situ hybridization. The gene consists of 13 exons separated by 12 introns and spans about 35 kilobases. Further sequence analysis and mapping showed that this locus contained three transglutaminase genes arranged in tandem:EPB42 (band 4.2 protein), TGM5, and a novel gene (TGM7). A full-length cDNA for the novel transglutaminase (TGZ) was obtained by anchored polymerase chain reaction. The deduced amino acid sequence encoded a protein with 710 amino acids and a molecular mass of 80 kDa. Northern blotting showed that the three genes are differentially expressed in human tissues. Band 4.2 protein expression was associated with hematopoiesis, whereas TGX and TGZ showed widespread expression in different tissues. Interestingly, the chromosomal segment containing the human TGM5, TGM7, andEPB42 genes and the segment containing the genes encoding TGC,TGE, and another novel gene (TGM6) on chromosome 20q11 are in mouse all found on distal chromosome 2 as determined by radiation hybrid mapping. This finding suggests that in evolution these six genes arose from local duplication of a single gene and subsequent redistribution to two distinct chromosomes in the human genome. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M102553200 |