ASSIGNMENT OF THE HUMAN HOMOLOG OF THE MTRIC-P5 GENE (TRIC5) TO BAND 1Q23 BY FLUORESCENCE IN-SITU HYBRIDIZATION

Citation
G. Sevigny et al., ASSIGNMENT OF THE HUMAN HOMOLOG OF THE MTRIC-P5 GENE (TRIC5) TO BAND 1Q23 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Genomics, 22(3), 1994, pp. 634-636
Citations number
16
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
08887543
Volume
22
Issue
3
Year of publication
1994
Pages
634 - 636
Database
ISI
SICI code
0888-7543(1994)22:3<634:AOTHHO>2.0.ZU;2-8
Abstract
The TCP1 ring complex (TRiC) is a molecular chaperone involved in acti n and tubulin folding. Little is known about the components of this co mplex. The first component identified was TCP1, a protein coded by a g ene in the t-complex locus on mouse chromosome 17. This locus is invol ved in several embryonic defects, male sterility, and the transmission ratio distortion. In humans, the t-complex genes map to chromosome 6. Other components of TRiC are thought to be TCP1-related proteins. Rec ently, a mouse cDNA coding for one of these proteins has been cloned a nd named mTRiC-P5. Here we report the cloning of a partial human cDNA clone, homologous to mTRiC-P5, and its chromosome localization by fluo rescence in situ hybridization. The human TRiC-P5 gene (TRIC5) maps to human chromosome 1q23, a region known to be a preferential chromosoma l breakpoint involved in leukemia. Therefore, even if TCP1 and TRiC-P5 are related proteins and are found in the same protein complex, they are not coded by syntenic genes in humans. (C) 1994 Academic Press, In c.