MER1, a yeast gene required for chromosome pairing and genetic recombination, is induced in meiosis

The yeast MER1 gene is required for the production of viable meiotic products and for meiotic recombination. Cytological analysis of chromosome spreads from a mer1 mutant indicates that the MER1 gene product is also required for normal chromosome pairing. mer1 strains make axial elements, precursors to the synaptonemal complex; however, the chromosomes in most nuclei do not become fully synapsed. The DNA sequence of the MER1 coding region was determined; the MER1 open reading frame encodes a 270-amino-acid protein with a molecular mass of 31.1 kilodaltons. The MER1 protein shows limited sequence similarity to calmodulin. Expression of the MER1 gene was examined by RNA blot hybridization analysis and through the construction and analysis of mer1::lacZ fusion genes. Expression of the MER1 gene is meiotically induced and required the IME1 gene product. Thus, expression of the MER1 gene early in meiosis is required for proper chromosome pairing and meiotic recombination.

[1]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[2]  G. Roeder,et al.  Transcription by RNA polymerase I stimulates mitotic recombination in Saccharomyces cerevisiae , 1989, Molecular and cellular biology.

[3]  H. E. Smith,et al.  A transcriptional cascade governs entry into meiosis in Saccharomyces cerevisiae , 1989, Molecular and cellular biology.

[4]  N. M. Hollingsworth,et al.  HOP1: a yeast meiotic pairing gene. , 1989, Genetics.

[5]  G. Roeder,et al.  Yeast mer1 mutants display reduced levels of meiotic recombination. , 1989, Genetics.

[6]  G. Roeder,et al.  Control of yeast gene expression by transposable elements: maximum expression requires a functional Ty activator sequence and a defective Ty promoter , 1988, Molecular and cellular biology.

[7]  Y. Kassir,et al.  IME1, a positive regulator gene of meiosis in S. cerevisiae , 1988, Cell.

[8]  M. Dresser,et al.  Meiotic chromosome behavior in spread preparations of yeast , 1988, The Journal of cell biology.

[9]  R. E. Esposito,et al.  Isolation, DNA sequence, and regulation of a meiosis-specific eukaryotic recombination gene. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[10]  A. Carpenter,et al.  Gene conversion, recombination nodules, and the initiation of meiotic synapsis. , 1987, BioEssays : news and reviews in molecular, cellular and developmental biology.

[11]  R. E. Esposito,et al.  Developmental regulation of SPO13, a gene required for separation of homologous chromosomes at meiosis I , 1987, Molecular and cellular biology.

[12]  W. Merrick,et al.  GTP-binding domain: three consensus sequence elements with distinct spacing. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[13]  B. Byers,et al.  Yeast gene required for spindle pole body duplication: homology of its product with Ca2+-binding proteins. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[14]  J. Berg,et al.  Potential metal-binding domains in nucleic acid binding proteins. , 1986, Science.

[15]  E. Chen,et al.  Shuttle mutagenesis: a method of transposon mutagenesis for Saccharomyces cerevisiae. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[16]  L. Guarente,et al.  Each of three "TATA elements" specifies a subset of the transcription initiation sites at the CYC-1 promoter of Saccharomyces cerevisiae. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[17]  G. Fink,et al.  The relationship between the "TATA" sequence and transcription initiation sites at the HIS4 gene of Saccharomyces cerevisiae. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[18]  R. E. Esposito,et al.  The role of the SPO11 gene in meiotic recombination in yeast. , 1985, Genetics.

[19]  A Klug,et al.  Repetitive zinc‐binding domains in the protein transcription factor IIIA from Xenopus oocytes. , 1985, The EMBO journal.

[20]  S. Henikoff Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. , 1984, Gene.

[21]  D. Gallwitz,et al.  Point mutations identify the conserved, intron-contained TACTAAC box as an essential splicing signal sequence in yeast , 1984, Cell.

[22]  K. Murata,et al.  Transformation of intact yeast cells treated with alkali cations. , 1984, Journal of bacteriology.

[23]  M. Rosbash,et al.  Evidence for the biochemical role of an internal sequence in yeast nuclear mRNA introns: Implications for U1 RNA and metazoan mRNA splicing , 1983, Cell.

[24]  E. H. Cohen,et al.  Transcription terminates in yeast distal to a control sequence , 1983, Cell.

[25]  R. W. Davis,et al.  RNA from the yeast transposable element Ty1 has both ends in the direct repeats, a structure similar to retrovirus RNA. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[26]  J. Woolford,et al.  Molecular cloning and analysis of the CRY1 gene: a yeast ribosomal protein gene. , 1983, Nucleic acids research.

[27]  J. Walker,et al.  Distantly related sequences in the alpha‐ and beta‐subunits of ATP synthase, myosin, kinases and other ATP‐requiring enzymes and a common nucleotide binding fold. , 1982, The EMBO journal.

[28]  F. Sherman,et al.  DNA sequence required for efficient transcription termination in yeast , 1982, Cell.

[29]  L Sikorski,et al.  Calmodulin , 2020, Definitions.

[30]  R. E. Esposito,et al.  Recombination and chromosome segregation during the single division meiosis in SPO12-1 and SPO13-1 diploids. , 1980, Genetics.

[31]  T. Vanaman,et al.  The complete amino acid sequence of the Ca2+-dependent modulator protein (calmodulin) of bovine brain. , 1980, The Journal of biological chemistry.

[32]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[33]  T. Manney,et al.  Expression of cryptopleurine resistance in Saccharomyces cerevisiae , 1977, Journal of bacteriology.

[34]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[35]  A. T. Carpenter Electron microscopy of meiosis in Drosophila melanogaster females: II. The recombination nodule--a recombination-associated structure at pachytene? , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[36]  D. Fast Sporulation Synchrony of Saccharomyces cerevisiae Grown in Various Carbon Sources , 1973, Journal of bacteriology.

[37]  J. C. Hall Chromosome segregation influenced by two alleles of the meiotic mutant c(3)G in Drosophila melanogaster. , 1972, Genetics.

[38]  R. King,et al.  Genetic control of synaptonemal complexes in Drosophila melanogaster. , 1968, Genetics.

[39]  D. Melton,et al.  In vitro RNA synthesis with SP6 RNA polymerase. , 1987, Methods in enzymology.

[40]  R. Sauer,et al.  Protein-DNA recognition. , 1984, Annual review of biochemistry.

[41]  S. W. Rasmussen,et al.  The synaptonemal complex in genetic segregation. , 1984, Annual review of genetics.

[42]  K. Struhl The new yeast genetics , 1983, Nature.

[43]  R. Rothstein One-step gene disruption in yeast. , 1983, Methods in enzymology.

[44]  Gerald R. Fink,et al.  Methods in Yeast Genetics: Laboratory Manual , 1981 .

[45]  J. Broach,et al.  The Molecular biology of the yeast saccharomyces, life cycle and inheritance , 1981 .

[46]  M. Resnick,et al.  The Role of Radiation (rad) Genes in Meiotic Recombination in Yeast. , 1980, Genetics.

[47]  B. S. Baker,et al.  The genetic control of meiosis. , 1976, Annual review of genetics.

[48]  I. Bogdanov [Synaptonemal complex]. , 1971, Tsitologiia.