Dmc1 of Schizosaccharomyces pombe plays a role in meiotic recombination

被引:41
作者
Fukushima, K [1 ]
Tanaka, Y [1 ]
Nabeshima, K [1 ]
Yoneki, T [1 ]
Tougan, T [1 ]
Tanaka, S [1 ]
Nojima, H [1 ]
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Mol Genet, Suita, Osaka 5650871, Japan
关键词
D O I
10.1093/nar/28.14.2709
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 report here a Schizosaccharomyces pombe gene (dmc1(+)) that resembles budding yeast DMC1 in the region immediately upstream of the rad24(+) gene. We showed by northern and Southern blot analysis that dmc1(+) and rad24(+) are co-transcribed as a bicistronic mRNA of 2.8 kb with meiotic specificity, whereas rad24(+) itself is constitutively transcribed as a 1.0-kb mRNA species during meiosis, Induction of the bicistronic transcript is under the control of a meiosis-specific transcription factor, Ste11, Disruption of both dmc1(+) and rad24(+) had no effect on mitosis or spore formation, and dmc1 Delta cells displayed no change in sensitivity to UV or gamma irradiation relative to the wild type. Tetrad analysis indicated that Dmc1 is involved in meiotic recombination, Analysis of gene conversion frequencies using single and double mutants of dmc1 and rhp51 indicated that both Dmc1 and Rhp51 function in meiotic gene conversion. These observations, together with a high level of sequence identity, indicate that the dmc1(+) gene of S.pombe is a structural homolog of budding yeast DMC1, sharing both similar and distinct functions in meiosis.
引用
收藏
页码:2709 / 2716
页数:8
相关论文
共 30 条
[1]   14-3-3 and its possible role in co-ordinating multiple signalling pathways [J].
Aitken, A .
TRENDS IN CELL BIOLOGY, 1996, 6 (09) :341-347
[2]   IDENTIFICATION AND CHARACTERIZATION OF NEW ELEMENTS INVOLVED IN CHECKPOINT AND FEEDBACK CONTROLS IN FISSION YEAST [J].
ALKHODAIRY, F ;
FOTOU, E ;
SHELDRICK, KS ;
GRIFFITHS, DJF ;
LEHMANN, AR ;
CARR, AM .
MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (02) :147-160
[3]   RECA HOMOLOGS DMC1 AND RAD51 INTERACT TO FORM MULTIPLE NUCLEAR-COMPLEXES PRIOR TO MEIOTIC CHROMOSOME SYNAPSIS [J].
BISHOP, DK .
CELL, 1994, 79 (06) :1081-1092
[4]   DMC1 - A MEIOSIS-SPECIFIC YEAST HOMOLOG OF ESCHERICHIA-COLI RECA REQUIRED FOR RECOMBINATION, SYNAPTONEMAL COMPLEX-FORMATION, AND CELL-CYCLE PROGRESSION [J].
BISHOP, DK ;
PARK, D ;
XU, LZ ;
KLECKNER, N .
CELL, 1992, 69 (03) :439-456
[5]  
Fantes P., 1993, Experiments with Fission Yeast
[6]   14-3-3-PROTEIN HOMOLOGS REQUIRED FOR THE DNA-DAMAGE CHECKPOINT IN FISSION YEAST [J].
FORD, JC ;
ALKHODAIRY, F ;
FOTOU, E ;
SHELDRICK, KS ;
GRIFFITHS, DJF ;
CARR, AM .
SCIENCE, 1994, 265 (5171) :533-535
[7]  
GRIMM C, 1994, GENETICS, V136, P41
[8]   GENETIC-ENGINEERING OF SCHIZOSACCHAROMYCES-POMBE - A SYSTEM FOR GENE DISRUPTION AND REPLACEMENT USING THE URA4 GENE AS A SELECTABLE MARKER [J].
GRIMM, C ;
KOHLI, J ;
MURRAY, J ;
MAUNDRELL, K .
MOLECULAR & GENERAL GENETICS, 1988, 215 (01) :81-86
[9]  
Gutz H., 1974, HDB GENETICS, V1, P395
[10]   The mouse and human homologs of DMC1, the yeast meiosis-specific homologous recombination gene, have a common unique form of exon-skipped transcript in meiosis [J].
Habu, T ;
Taki, T ;
West, A ;
Nishimune, Y ;
Morita, T .
NUCLEIC ACIDS RESEARCH, 1996, 24 (03) :470-477