Nucleic Acids Research, Vol 26, Issue 9 2063-2068, Copyright © 1998 by Oxford University Press
O Imamura, K Saiki, T Tani, Y Ohshima, M Sugawara and Y Furuichi
During the splicing process, spliceosomal snRNAs undergo numerous
conformational rearrangements that appear to be catalyzed by proteins
belonging to the DEAD/H-box superfamily of RNA helicases. We have cloned a
new RNA helicase gene, designated DBP2 (DEAH-boxprotein), homologous to the
Schizosaccaromyces pombe cdc28(+)/prp8(+) gene involved in pre-mRNA
splicing and cell cycle progression. The full- length DBP2 contains 3400
nucleotides and codes for a protein of 1041 amino acids with a calculated
mol. wt of 119 037 Da. Transfection experiments demonstrated that the
GFP-DBP2 gene product, transiently expressed in HeLa cells, was localized
in the nucleus. The DBP2 gene was mapped by FISH to the MHC region on human
chromosome 6p21.3, a region where many malignant, genetic and autoimmune
disease genes are linked. Because the expression of DBP2 gene in S.pombe
prp8 mutant cells partially rescued the temperature-sensitive phenotype, we
conclude that DBP2 is a functional human homolog of the fission yeast
Cdc28/Prp8 protein.
ARTICLES
Cloning and characterization of a human DEAH-box RNA helicase, a functional homolog of fission yeast Cdc28/Prp8
AGENE Research Institute, 200 Kajiwara, Kamakura 247-0063, Japan.
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