ライフサイエンスコーパス: mating type gene

1 lactis, which contains cryptic copies of the mating type genes.

2 mologs elicited sexual reactions like native mating-type genes.

3 r4p, Chp1p is not required to repress silent mating-type genes.

4 urally silenced endogenous HMRa and HMLalpha mating type genes, acts downstream of gene activator pro

5 rgely attributable to derepression of silent mating-type genes, although Sir proteins do play a minor

6 ry mating types in nature, the expression of mating type genes and evidence of recent genome recombin

7 plicated in the silencing both of the silent mating type genes and of genes within the ribosomal DNA

8 d in the Rap1p-mediated repression of silent mating type genes and of telomere-proximal genes, do not

9 shroom Coprinus cinereus, the multiallelic B mating type genes are predicted to encode a large family

10 The products of the mating-type genes are the master regulators of sexual de

11 rproduction of Sas10p caused derepression of mating type genes at both HML and HMR, as well as of URA

12 hallism), is determined by the expression of mating type genes at mat loci.

13 u70 and Sir1 act collectively to silence the mating-type genes at HML and HMR.

14 of homokaryotic mushrooms appears to bypass mating type gene control.

15 The existence of strata devoid of mating-type genes, despite the lack of sexual antagonism

16 ional sex-related genes, the distribution of mating-type genes, detection of recombination from popul

17 In Schizophyllum, tightly linked Y and Z mating-type genes do not promote development in the comb

18 bility and growth, that a solitary Z A alpha mating-type gene does not itself activate development, t

19 molecular basis of homothallism and role of mating type genes during a self-fertile sexual cycle rem

20 s for receptors, pheromones, G proteins, and mating type genes during fusion of opposite mating-type

21 Thus, SIR genes, which repress silent mating type gene expression, are required for the adapta

22 Differences in mating-type gene expression in haploid and diploid cells

23 uding aerobically repressed hypoxic genes, a-mating type genes, glucose repressed genes, and genes co

24 transcription factor and pheromone receptor mating-type gene homologs from C. disseminatus.

25 gulation and molecular functions of the matA mating type gene in a homothallic system.

26 g balancing selection and apply it to the b1 mating type gene in the mushroom fungus Coprinus cinereu

27 Tsong et al. characterize the role of mating type genes in Candida albicans and identify a new

28 pansions of recombination suppression beyond mating-type genes in fungi ('evolutionary strata'), whic

29 se is still uncertain, but recent studies of mating-type genes in green algae open a promising new wa

30 attention has been paid to the switching of mating-type genes in Saccharomyces cerevisiae, a process

31 cleation sites flanking silent copies of the mating-type genes in Saccharomyces cerevisiae.

32 Furthermore, the MAT1-1-1 mating-type gene, known primarily for a role in governin

33 of transcriptional silencing at the cryptic mating-type gene loci in Saccharomyces cerevisiae.

34 Mating-type gene (MAT) switching in budding yeast exhibi

35 and pheromones control sexual identity, the mating-type genes (mat A and mat a) must be in two diffe

36 MTL) of both of the Saccharomyces cerevisiae mating-type genes (MAT) a and alpha.

37 fertile and self-sterile strains, found four mating type genes (MAT1-1-1, MAT1-1-5, MAT1-2-1 and MAT1

38 The Aspergillus nidulans mating type gene matA and the human SRY (Sex-Determining

39 Repression of mating-type genes occurs when Tup1-Ssn6 is brought to th

40 The A mating type-genes of the mushroom, Coprinus cinereus, en

41 enome sequence also revealed the presence of mating-type genes, providing an indication that Malassez

42 t silences transcription of the alpha- and a-mating-type genes, respectively.

43 The mating-type genes, which encode pheromones, pheromone re