Gough N M, Gearing D P, King J A, Willson T A, Hilton D J, Nicola N A, Metcalf D
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.
Proc Natl Acad Sci U S A. 1988 Apr;85(8):2623-7. doi: 10.1073/pnas.85.8.2623.
A human homologue of the recently cloned murine leukemia-inhibitory factor (LIF) gene was isolated from a genomic library by using the murine cDNA as a hybridization probe. The nucleotide sequence of the human gene indicated that human LIF has 78% amino acid sequence identity with murine LIF, with no insertions or deletions, and that the region of the human gene encoding the mature protein has one intervening sequence. After oligonucleotide-mediated mutagenesis, the mature protein-coding region of the LIF gene was introduced into the yeast expression vector YEpsec1. Yeast cells transformed with the resulting recombinant could be induced with galactose to produce high levels of a factor that induced the differentiation of murine M1 leukemic cells in a manner analogous to murine LIF. This factor competed with 125I-labeled native murine LIF for binding to specific cellular receptors on murine cells, compatible with a high degree of structural similarity between the murine and human factors.
通过使用鼠源cDNA作为杂交探针,从基因组文库中分离出了最近克隆的鼠白血病抑制因子(LIF)基因的人类同源物。人类基因的核苷酸序列表明,人类LIF与鼠LIF具有78%的氨基酸序列同一性,没有插入或缺失,并且人类基因编码成熟蛋白的区域有一个间隔序列。经过寡核苷酸介导的诱变后,LIF基因的成熟蛋白编码区被引入酵母表达载体YEpsec1。用所得重组体转化的酵母细胞可用半乳糖诱导,以产生高水平的一种因子,该因子以类似于鼠LIF的方式诱导鼠M1白血病细胞分化。该因子与125I标记的天然鼠LIF竞争结合鼠细胞上的特异性细胞受体,这与鼠和人类因子之间高度的结构相似性相符。