Ray D, Bosselut R, Ghysdael J, Mattei M G, Tavitian A, Moreau-Gachelin F
Faculté de Médecine Lariboisière Saint-Louis, INSERM U-248, Paris, France.
Mol Cell Biol. 1992 Oct;12(10):4297-304. doi: 10.1128/mcb.12.10.4297-4304.1992.
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.
我们基于与Spi-1/PU.1假定癌基因产物的DNA结合域的同源性,从一个新基因spi-B中克隆了一条人类cDNA。spi-B编码一种由262个氨基酸组成的蛋白质,与Spi-1的整体一致性为43%。其高度碱性的羧基末端区域与Ets-1蛋白的DNA结合域具有34%的序列一致性。我们发现Spi-B蛋白能够结合Spi-1/PU.1识别的富含嘌呤的序列(PU盒),并激活含有PU盒的报告质粒的转录。染色体原位杂交使我们能够将spi-B定位到人类基因组的19q13.3-19q13.4区域。与spi-1一样,除了T淋巴细胞系外,spi-B在各种小鼠和人类造血细胞系中均有表达。