z-logo
open-access-imgOpen Access
Characterization of Spi-B, a transcription factor related to the putative oncoprotein Spi-1/PU.1.
Author(s) -
Ray D,
Rémy Bosselut,
Jacques Ghysdael,
MarieGeneviève Mattéi,
A Tavitian,
Françoise Moreau-Gachelin
Publication year - 1992
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.12.10.4297
Subject(s) - biology , microbiology and biotechnology , complementary dna , gene , ddb1 , homology (biology) , transcription factor , dna binding protein , peptide sequence , transcription (linguistics) , dna , genetics , linguistics , philosophy
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom