The complete sequence of a 6794 bp segment located on the right arm of chromosome II ofSaccharomyces cerevisiae. Finding of a putative dUTPase in a yeast

Yeast ◽  
1993 ◽  
Vol 9 (10) ◽  
pp. 1131-1137 ◽  
Author(s):  
Francois Doignon ◽  
Nicolas Biteau ◽  
Michel Aigle ◽  
Marc Crouzet
Keyword(s):  
Complete Sequence ◽  
The Right ◽  
Chromosome Ii

The complete sequence of a 19,482 bp segment located on the right arm of Chromosome II fromSaccharomyces cerevisiae

Yeast ◽  
1993 ◽  
Vol 9 (2) ◽  
pp. 189-199 ◽  
Author(s):  
Francois Doignon ◽  
Nicolas Biteau ◽  
Marc Crouzet ◽  
Michel Aigle
Keyword(s):  
Complete Sequence ◽  
The Right ◽  
Chromosome Ii

The complete sequence of a 10·8kb fragment to the right of the chromosome III centromere ofSaccharomyces cerevisiae

Yeast ◽  
1992 ◽  
Vol 8 (1) ◽  
pp. 61-70 ◽  
Author(s):  
Nicolas Biteau ◽  
Christophe Fremaux ◽  
Sylvie Hebrard ◽  
Annie Menara ◽  
Michael Aigle ◽  
...  
Keyword(s):  
Complete Sequence ◽  
Chromosome Iii ◽  
The Right

The complete sequence of a 9037 bp DNA fragment of the right arm ofSaccharomyces cerevisiae chromosome VII

Yeast ◽  
1995 ◽  
Vol 11 (6) ◽  
pp. 587-591 ◽  
Author(s):  
Javier Arroyo ◽  
Melba García-Gonzalez ◽  
M. Isabel García-Saez ◽  
Miguel Sánchez ◽  
César Nombela
Keyword(s):  
Complete Sequence ◽  
Dna Fragment ◽  
The Right

II. Yeast sequencing reports. Analysis of a 70kb region on the right arm of yeast chromosome II

Yeast ◽  
1994 ◽  
Vol 10 (10) ◽  
pp. 1363-1381 ◽  
Author(s):  
Gertrud Mannhaupt ◽  
Rolf Stucka ◽  
Susanne Ehnle ◽  
Irene Vetter ◽  
Horst Feldmann
Keyword(s):  
Yeast Chromosome ◽  
The Right ◽  
Chromosome Ii

Towards the cloning of GLY1

2000 ◽  
Vol 28 (6) ◽  
pp. 675-677 ◽  
Author(s):  
M. Miquel
Keyword(s):  
Carbon Flux ◽  
Biochemical Study ◽  
Complete Sequence ◽  
Chromosome Walking ◽  
Ethyl Methane Sulphonate ◽  
Methane Sulphonate ◽  
Glycerol Treatment ◽  
Phosphate Supply ◽  
Chromosome Ii ◽  
Map Location

The Arabidopsis mutants designated gly1 exhibit a reduced carbon flux through the prokaryotic pathway that is compensated for by an increased carbon flux through the eukaryotic pathway. Biochemical approaches reveal that the gly1 phenotype cannot be explained by a deficiency in the enzymes of the prokaryotic pathway. The chemical complementation of the mutant phenotype by exogenous glycerol treatment of gly1 plants suggests a lesion affecting the glycerol 3-phosphate supply within the chloroplast. As an alternative to the biochemical study of the gly1 mutants we set out to map the GLY1 locus. The gly1 mutant being an EMS (ethyl methane sulphonate) mutant, we used a strategy based on the polymorphism existing between Arabidopsis ecotypes, here Columbia (gly1 background) and Landsberg erecta. We mapped gly1 on chromosome II. During the process of chromosome walking, the complete sequence of chromosome II was released, allowing us to make assumptions on candidate genes based on map location. We are currently sequencing the putative genes.

The clr1 locus regulates the expression of the cryptic mating-type loci of fission yeast.

Genetics ◽  
1992 ◽  
Vol 131 (2) ◽  
pp. 287-296 ◽  
Author(s):  
G Thon ◽  
A J Klar
Keyword(s):  
Fission Yeast ◽  
Mating Type ◽  
Cold Spot ◽  
Type Region ◽  
Type Locus ◽  
Silent Genes ◽  
The Right ◽  
Chromosome Ii ◽  
Donor Locus ◽  
Type Information

Abstract The mat2-P and mat3-M loci of fission yeast contain respectively the plus (P) and minus (M) mating-type information in a transcriptionally silent state. That information is transposed from the mat2 or mat3 donor locus via recombination into the expressed mating-type locus (mat1) resulting in switching of the cellular mating type. We have identified a gene, named clr1 (for cryptic loci regulator), whose mutations allow expression of the mat2 and mat3 loci. clr1 mutants undergo aberrant haploid meiosis, indicative of transcription of the silent genes. Production of mRNA from mat3 is detectable in clr1 mutants. Furthermore, the ura4 gene inserted near mat3, weakly expressed in wild-type cells, is derepressed in clr1 mutants. The clr1 mutations also permit meiotic recombination in the 15-kb mat2-mat3 interval, where recombination is normally inhibited. The clr1 locus is in the right arm of chromosome II. We suggest that clr1 regulates silencing of the mat2 and mat3 loci, and participates in establishing the "cold spot" for recombination by organizing the chromatin structure of the mating-type region.

Analysis of 41 kb of the DNA sequence from the right arm of chromosome II ofSchizosaccharomyces pombe

Yeast ◽  
2001 ◽  
Vol 18 (12) ◽  
pp. 1111-1116 ◽  
Author(s):  
Manuel Sánchez ◽  
José L. Revuelta ◽  
Francisco del Rey ◽  
Rhian Gwilliam ◽  
Jason Skelton ◽  
...  
Keyword(s):  
Dna Sequence ◽  
The Right ◽  
Chromosome Ii

II. Yeast sequencing reports. Sequence analysis of a 31 kb DNA fragment from the right arm ofSaccharomyces cerevisiae chromosome II

Yeast ◽  
1994 ◽  
Vol 10 (7) ◽  
pp. 959-964 ◽  
Author(s):  
Quirina J. M. Van Der Aart ◽  
H. Ydesteensma ◽  
Christophe Barthe ◽  
François Doignon ◽  
Michel Aigle ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
Dna Fragment ◽  
The Right ◽  
Chromosome Ii

scholarly journals STRUCTURAL ANALYSIS OF THE dur LOCI IN S. CEREVISIAE: TWO DOMAINS OF A SINGLE MULTIFUNCTIONAL GENE

Genetics ◽  
1980 ◽  
Vol 94 (3) ◽  
pp. 555-580 ◽  
Author(s):  
Terrance G Cooper ◽  
Christine Lam ◽  
Vanessa Turoscy
Keyword(s):  
Carbon Dioxide ◽  
Saccharomyces Cerevisiae ◽  
Structural Analysis ◽  
Single Gene ◽  
The Right ◽  
Chromosome Ii

ABSTRACT In Saccharomyces cerevisiae, the degradation of urea to carbon dioxide and ammonia is catalyzed byurea carboxylase and albphanate hydrolase. The loci coding for these enzymes (dur1 and dur2) are very tightly linked an the right arm of chromosome II between pet11 and met8. Pleiotropic mutations that fail to complement mutations in either of the dur loci were found to be predominantly located in or near the dur2 locus. We interpret these data as suggesting that the two dur loci might in reality be domains of a single gene that codes fora multifunctional polypeptide. In view OIthis conclusion, we have renamed the dur loci as the durl,2 locus.

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