STRUCTURE, EXPRESSION AND CHROMOSOMAL LOCALIZATION OF HUMAN P80-COILIN GENE

被引:45
|
作者
CHAN, EKL
TAKANO, S
ANDRADE, LEC
HAMEL, JC
MATERA, AG
机构
[1] SCRIPPS RES INST, DEPT MOLEC & EXPTL MED, DNA CORE LAB STRUCT ANAL, LA JOLLA, CA 92037 USA
[2] CASE WESTERN RESERVE UNIV, DEPT GENET, CLEVELAND, OH 44106 USA
[3] CASE WESTERN RESERVE UNIV, CTR HUMAN GENET, CLEVELAND, OH 44106 USA
关键词
D O I
10.1093/nar/22.21.4462
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Coiled bodies (CBs) are non-capsular nuclear bodies with a diameter of 0.3-1 mu m and appear to be composed of coiled fibrils. Human autoantibodies to CBs recognize an 80-kD nuclear protein highly enriched in CBs, and this protein has been named p80-coilin. CBs are known to assemble and disassemble during the cell cycle, with the highest number of CBs occurring at mid to late G(1) where p80-coilin is assembled into several small nuclear body-like structures. In S and G(2) phases, CBs become larger and their number decreases and often they are undetectable during mitosis. Using a human autoantibody as a probe for expression cloning, we initially isolated a partial cDNA encoding p80-coilin. In this report, the 5' end of the complete cDNA for p80-coilin was obtained using the 5'-RACE (rapid amplification of cDNA ends) methodology. The size of the reconstructed full-length cDNA corresponds to the 2.7-kb mRNA detected in Northern blot analysis. The complete p80-coilin protein consists of 576 amino acids with a predicted molecular mass of 62,608. A putative p80-coilin pseudogene was also detected during the rescreening of p80-coilin cDNA. To confirm the validity of the cDNA sequence, three overlapping genomic DNA clones representing the human p80-coilin gene were selected for further analysis. The complete gene for p80-coilin contains 7 exons spanning similar to 25kb. Sequence analysis of exons 1 and 2 in genomic DNA clones confirmed the accuracy of the 5' cDNA sequence derived from the 5'-RACE procedure. Furthermore, the human p80-coilin gene was localized to chromosome 17q22-23 by fluorescence in situ hybridization.
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页码:4462 / 4469
页数:8
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