CHARACTERIZATION OF SPI-B, A TRANSCRIPTION FACTOR RELATED TO THE PUTATIVE ONCOPROTEIN SPI-1/PU.1

被引:169
作者
RAY, D
BOSSELUT, R
GHYSDAEL, J
MATTEI, MG
TAVITIAN, A
MOREAUGACHELIN, F
机构
[1] FAC MED LARIBOISIERE,INSERM U248,10 AVE VERDUN,F-75010 PARIS,FRANCE
[2] HOP ENFANTS LA TIMONE,INSERM,U-242,F-13385 MARSEILLE,FRANCE
[3] INST CURIE,BIOL SECT,ONCOL VIRALE & CELLULAIRE LAB,F-91405 ORSAY,FRANCE
关键词
D O I
10.1128/MCB.12.10.4297
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
We have cloned a human cDNA from a new gene, spi-B, on the basis of its homology with the DNA-binding domain of the Spi-1/PU.1 putative oncogene product. spi-B codes for a protein of 262 amino acids presenting 43% overall identity with Spi-1. Its highly basic carboxy-terminal region exhibits 34% sequence identity with the DNA-binding domain of the Ets-1 protein. We showed that the Spi-B protein is able to bind the purine-rich sequence (PU box) recognized by Spi-1/PU.1 and to activate transcription of a reporter plasmid containing PU boxes. Chromosome in situ hybridization allowed us to map spi-B to the 19q13.3-19q13.4 region of the human genome. spi-B, like spi-1, was found to be expressed in various murine and human hematopoietic cell lines except T lymphoid cell lines.
引用
收藏
页码:4297 / 4304
页数:8
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