scholarly journals A genomic clone of Zfy-1 from a YDOM mouse strain detects post-meiotic gene expression of Zfy in testes

1989 ◽  
Vol 165 (3) ◽  
pp. 1286-1291 ◽  
Author(s):  
Linda M. Kalikin ◽  
Hirokazu Fujimoto ◽  
Michal P. Witt ◽  
Vera Verga ◽  
Robert P. Erickson
2005 ◽  
Vol 25 (2) ◽  
pp. 302-308 ◽  
Author(s):  
Raymond Tabibiazar ◽  
Roger A. Wagner ◽  
Joshua M. Spin ◽  
Euan A. Ashley ◽  
Balasubramanian Narasimhan ◽  
...  

2010 ◽  
Vol 285 (36) ◽  
pp. 27859-27868 ◽  
Author(s):  
Olivier St-André ◽  
Caroline Lemieux ◽  
Audrey Perreault ◽  
Daniel H. Lackner ◽  
Jürg Bähler ◽  
...  

1995 ◽  
Vol 15 (10) ◽  
pp. 5279-5287 ◽  
Author(s):  
R A Sia ◽  
A P Mitchell

Ime2p is a protein kinase that is expressed only during meiosis in Saccharomyces cerevisiae. Ime2p stimulates early, middle, and late meiotic gene expression and down-regulates expression of IME1, which specifies an activator of early meiotic genes that acts independently of Ime2p. We have identified a new gene, IDS2 (for IME2-dependent signaling), which has a functional relationship to Ime2p. An ids2 null mutation delays down-regulation of IME1 and expression of middle and late meiotic genes. In an ime1 null mutant that express IME2 from the GAL1 promoter (ime1 delta PGAL1-IME2 mutant), early meiotic gene expression depends only upon Ime2p. In such strains, Ids2p is dispensable for expression of the early genes HOP1 and SPO13 but is essential for expression of the middle and late genes SPS1, SPS2, and SPS100. Ids2p is also essential for the autoregulatory pathway through which Ime2p activates its own expression via the IME2 upstream activation sequences (UAS). An PGAL1-IME2 derivative that produces a truncated Ime2p (lacking its C-terminal 174 residues) permits IME2 UAS activation in the absence of Ids2p. This observation suggests that Ids2p acts upstream of Ime2p or that Ids2p and Ime2p act in independent, convergent pathways to stimulate IME2 UAS activity. Accumulation of epitope-tagged Ids2p derivatives is greatest in growing cells and declines during meiosis. We propose that Ids2p acts indirectly to modify Ime2p activity, thus permitting Ime2p to carry out later meiotic functions.


2012 ◽  
Vol 5 (1) ◽  
pp. 232 ◽  
Author(s):  
Petra Kraus ◽  
Xing Xing ◽  
Siew Lim ◽  
Max E Fun ◽  
V Sivakamasundari ◽  
...  

Genetics ◽  
2001 ◽  
Vol 157 (3) ◽  
pp. 1179-1189 ◽  
Author(s):  
Luther Davis ◽  
Maria Barbera ◽  
Amanda McDonnell ◽  
Katherine McIntyre ◽  
Rolf Sternglanz ◽  
...  

Abstract The Saccharomyces cerevisiae MUM2 gene is essential for meiotic, but not mitotic, DNA replication and thus sporulation. Genetic interactions between MUM2 and a component of the origin recognition complex and polymerase α-primase suggest that MUM2 influences the function of the DNA replication machinery. Early meiotic gene expression is induced to a much greater extent in mum2 cells than in meiotic cells treated with the DNA synthesis inhibitor hydroxyurea. This result indicates that the mum2 meiotic arrest is downstream of the arrest induced by hydroxyurea and suggests that DNA synthesis is initiated in the mutant. Genetic analyses indicate that the recombination that occurs in mum2 mutants is dependent on the normal recombination machinery and on synaptonemal complex components and therefore is not a consequence of lesions created by incompletely replicated DNA. Both meiotic ectopic and allelic recombination are similarly reduced in the mum2 mutant, and the levels are consistent with the levels of meiosis-specific DSBs that are generated. Cytological analyses of mum2 mutants show that chromosome pairing and synapsis occur, although at reduced levels compared to wild type. Given the near-wild-type levels of meiotic gene expression, pairing, and synapsis, we suggest that the reduction in DNA replication is directly responsible for the reduced level of DSBs and meiotic recombination.


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