Literature DB >> 2249774

Isolation of two developmentally regulated genes involved in spore wall maturation in Saccharomyces cerevisiae.

P Briza1, M Breitenbach, A Ellinger, J Segall.   

Abstract

During sporulation of Saccharomyces cerevisiae, the four haploid nuclei generated by meiosis are encapsulated within multilayered spore walls. Taking advantage of the natural fluorescence imparted to yeast spores by the presence of a dityrosine-containing macromolecule in the spore wall, we identified and cloned two genes, termed DIT1 and DIT2, which are required for spore wall maturation. Mutation of these genes has no effect on the efficiency of spore formation or spore viability. The mutant spores, however, fail to accumulate the spore wall-specific dityrosine and lack the outermost layer of the spore wall. The absence of this cross-linked surface layer reduces the resistance of the spores to lytic enzymes, to ether, and to elevated temperature. Expression of the DIT and DIT2 genes is restricted to sporulating cells, with the DIT1 transcripts accumulating at the time of prospore enclosure and just prior to the time of dityrosine biosynthesis. Both genes act in a spore-autonomous manner implying that at least some of the activities responsible for forming the outermost layer of the spore wall reside within the developing spore rather than in the surrounding ascal cytoplasm. As the DIT2 gene product has significant homology with cytochrome P-450s, DIT2 may be responsible for catalyzing the oxidation of tyrosine residues in the formation of dityrosine.

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Year:  1990        PMID: 2249774     DOI: 10.1101/gad.4.10.1775

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  90 in total

1.  Role for the silencing protein Dot1 in meiotic checkpoint control.

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2.  The CDK-activating kinase CAK1 can dosage suppress sporulation defects of smk1 MAP kinase mutants and is required for spore wall morphogenesis in Saccharomyces cerevisiae.

Authors:  M Wagner; M Pierce; E Winter
Journal:  EMBO J       Date:  1997-03-17       Impact factor: 11.598

3.  The Smk1p MAP kinase negatively regulates Gsc2p, a 1,3-beta-glucan synthase, during spore wall morphogenesis in Saccharomyces cerevisiae.

Authors:  Linda S Huang; Hugh K Doherty; Ira Herskowitz
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-22       Impact factor: 11.205

4.  Morphogenetic pathway of spore wall assembly in Saccharomyces cerevisiae.

Authors:  Alison Coluccio; Edith Bogengruber; Michael N Conrad; Michael E Dresser; Peter Briza; Aaron M Neiman
Journal:  Eukaryot Cell       Date:  2004-12

Review 5.  Ascospore formation in the yeast Saccharomyces cerevisiae.

Authors:  Aaron M Neiman
Journal:  Microbiol Mol Biol Rev       Date:  2005-12       Impact factor: 11.056

6.  Identification of a sporulation-specific promoter regulating divergent transcription of two novel sporulation genes in Saccharomyces cerevisiae.

Authors:  J G Coe; L E Murray; I W Dawes
Journal:  Mol Gen Genet       Date:  1994-09-28

7.  Spe3, which encodes spermidine synthase, is required for full repression through NRE(DIT) in Saccharomyces cerevisiae.

Authors:  H Friesen; J C Tanny; J Segall
Journal:  Genetics       Date:  1998-09       Impact factor: 4.562

8.  The sporulation-specific enzymes encoded by the DIT1 and DIT2 genes catalyze a two-step reaction leading to a soluble LL-dityrosine-containing precursor of the yeast spore wall.

Authors:  P Briza; M Eckerstorfer; M Breitenbach
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-10       Impact factor: 11.205

9.  Phosphorylation and maximal activity of Saccharomyces cerevisiae meiosis-specific transcription factor Ndt80 is dependent on Ime2.

Authors:  Richelle Sopko; Sheetal Raithatha; David Stuart
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

10.  Prenylated isoforms of yeast casein kinase I, including the novel Yck3p, suppress the gcs1 blockage of cell proliferation from stationary phase.

Authors:  X Wang; M F Hoekstra; A J DeMaggio; N Dhillon; A Vancura; J Kuret; G C Johnston; R A Singer
Journal:  Mol Cell Biol       Date:  1996-10       Impact factor: 4.272

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