Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
Analysis of the EBI/GeneBank TM data base using non-human hair keratin-associated protein (KAP) cDNA sequences as a query resulted in the identification of a first domain of high glycine-tyrosine and high sulfur KAP genes located on human chromosome 21q22.1. This domain, present on the DNA accession...
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Published in | The Journal of biological chemistry Vol. 277; no. 50; pp. 48993 - 49002 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Biochemistry and Molecular Biology
13.12.2002
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Subjects | |
Online Access | Get full text |
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Summary: | Analysis of the EBI/GeneBank TM data base using non-human hair keratin-associated protein (KAP) cDNA sequences as a query resulted in the identification
of a first domain of high glycine-tyrosine and high sulfur KAP genes located on human chromosome 21q22.1. This domain, present
on the DNA accession numbers AP001078 and AP001709 , was â¼535 kb in size and contained 17 high glycine-tyrosine and 7 high sulfur KAP genes, as well as 9 KAP pseudogenes. Based
on amino acid sequence comparisons of the encoded proteins, the KAP genes could be divided into seven high glycine-tyrosine
gene families (KAP6âKAP8, and KAP19âKAP22) and four high sulfur gene families (KAP11, KAP13, KAP15, and KAP23). The high glycine-tyrosine
genes described here appear to represent the complete set of this type of KAP genes present in the human genome. Both systematic
cDNA isolation studies from an arrayed scalp cDNA library and in situ hybridization expression studies of all of the KAP genes identified in the 21q22.1 region revealed varying degrees and regions
of expression of 11 members of the high tyrosine-glycine genes and 6 members of the high sulfur KAP genes in the hair forming
compartment. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M206422200 |