CROSS-SPECIES COMPARISON OF THE SEQUENCE OF THE LEUKEMIA INHIBITORY FACTOR GENE AND ITS PROTEIN

被引:50
作者
WILLSON, TA
METCALF, D
GOUGH, NM
机构
[1] Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Parkville, Victoria, Post Office
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1992年 / 204卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1992.tb16601.x
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
Leukaemia inhibitory factor (LIF) is a pleiotropic growth factor active in diverse cell systems in both the adult and the embryo. The LIF gene from a number of mammalian species is highly conserved. The ovine and porcine LIF genes were cloned, sequenced and compared to the previously published murine and human LIF gene sequences. While the coding regions of the LIF gene are highly conserved, the non-coding regions are largely non-conserved. In a region of almost-equal-to 340 bp, the 5' end of the translational initiation codon is highly conserved (84%). This region includes four conserved TATA boxes, two transcriptional start-sites identified in the murine gene and the minimal region required to function as the LIF promoter. A sequence in the murine gene adjacent to this highly conserved region which appears to contain a negative control element is, however, poorly conserved between the four species compared, except for a sequence of 16 conserved nucleotides. Within the largely non-conserved first intron, there is a block of almost-equal-to 150 nucleotides which is highly conserved between all four species (almost-equal-to 72%). However, a sequence in intron 1 of the murine LIF gene which corresponds to an alternative exon of a putative variant LIF transcript is very poorly conserved between species, with only relics of this exon evident in the other three species. A comparison of the five LIF protein sequences available (murine, rat, human, ovine and porcine) revealed that the protein displays a high degree of similarity, ranging from 74% between mouse and sheep to 92% between rat and mouse. Several large blocks of absolutely conserved amino acid sequence were identified. The ovine LIF gene was modified to allow production of recombinant ovine LIF in yeast cells, which was shown to be biologically active on murine cells.
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页码:21 / 30
页数:10
相关论文
共 32 条
[1]   DIFFERENTIATION-INDUCING FACTOR PURIFIED FROM CONDITIONED MEDIUM OF MITOGEN-TREATED SPLEEN-CELL CULTURES STIMULATES BONE-RESORPTION [J].
ABE, E ;
TANAKA, H ;
ISHIMI, Y ;
MIYAURA, C ;
HAYASHI, T ;
NAGASAWA, H ;
TOMIDA, M ;
YAMAGUCHI, Y ;
HOZUMI, M ;
SUDA, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :5958-5962
[2]   A NOVEL LEADER PEPTIDE WHICH ALLOWS EFFICIENT SECRETION OF A FRAGMENT OF HUMAN INTERLEUKIN 1-BETA IN SACCHAROMYCES-CEREVISIAE [J].
BALDARI, C ;
MURRAY, JAH ;
GHIARA, P ;
CESARENI, G ;
GALEOTTI, CL .
EMBO JOURNAL, 1987, 6 (01) :229-234
[3]  
BAUMANN H, 1989, J IMMUNOL, V143, P1163
[4]   ALTERING THE GENOME BY HOMOLOGOUS RECOMBINATION [J].
CAPECCHI, MR .
SCIENCE, 1989, 244 (4910) :1288-1292
[5]   PEMBL - A NEW FAMILY OF SINGLE STRANDED PLASMIDS [J].
DENTE, L ;
CESARENI, G ;
CORTESE, R .
NUCLEIC ACIDS RESEARCH, 1983, 11 (06) :1645-1655
[6]   THE PROMOTER-SPECIFIC TRANSCRIPTION FACTOR-SP1 BINDS TO UPSTREAM SEQUENCES IN THE SV40 EARLY PROMOTER [J].
DYNAN, WS ;
TJIAN, R .
CELL, 1983, 35 (01) :79-87
[7]   MULTIPLE DNA-SEQUENCE ELEMENTS ARE NECESSARY FOR THE FUNCTION OF AN IMMUNOGLOBULIN HEAVY-CHAIN PROMOTER [J].
EATON, S ;
CALAME, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7634-7638
[8]   THE STRUCTURE AND EVOLUTION OF THE HUMAN BETA-GLOBIN GENE FAMILY [J].
EFSTRATIADIS, A ;
POSAKONY, JW ;
MANIATIS, T ;
LAWN, RM ;
OCONNELL, C ;
SPRITZ, RA ;
DERIEL, JK ;
FORGET, BG ;
WEISSMAN, SM ;
SLIGHTOM, JL ;
BLECHL, AE ;
SMITHIES, O ;
BARALLE, FE ;
SHOULDERS, CC ;
PROUDFOOT, NJ .
CELL, 1980, 21 (03) :653-668
[9]   MOLECULAR-CLONING AND EXPRESSION OF CDNA-ENCODING A MURINE MYELOID-LEUKEMIA INHIBITORY FACTOR (LIF) [J].
GEARING, DP ;
GOUGH, NM ;
KING, JA ;
HILTON, DJ ;
NICOLA, NA ;
SIMPSON, RJ ;
NICE, EC ;
KELSO, A ;
METCALF, D .
EMBO JOURNAL, 1987, 6 (13) :3995-4002
[10]  
GEARING DP, 1989, BIO-TECHNOL, V7, P1157