scholarly journals Genetic control of fission yeast cell wall synthesis: the genes involved in wall biogenesis and their interactions in Schizosaccharomyces pombe.

1998 ◽  
Vol 73 (4) ◽  
pp. 181-191 ◽  
Author(s):  
Junpei Ishiguro
2018 ◽  
Vol 4 ◽  
pp. 1-9 ◽  
Author(s):  
Pilar Pérez ◽  
Juan C.G. Cortés ◽  
Jose Cansado ◽  
Juan C. Ribas

2017 ◽  
Vol 2017 (11) ◽  
pp. pdb.top079897 ◽  
Author(s):  
Pilar Pérez ◽  
Juan C. Ribas

2015 ◽  
Vol 25 (16) ◽  
pp. 2150-2157 ◽  
Author(s):  
Erdinc Atilgan ◽  
Valentin Magidson ◽  
Alexey Khodjakov ◽  
Fred Chang

1969 ◽  
Vol 115 (2) ◽  
pp. 231-240 ◽  
Author(s):  
R. Sentandreu ◽  
D. H. Northcote

1. A study of wall synthesis has been made by following the incorporation of radioactive glucose and threonine into the cytoplasm and wall of yeast. 2. Both glucose and threonine are incorporated into a mannan glycopeptide. The glucose is also synthesized into a structural glucan of the wall. 3. The mannan glycopeptide contains high-molecular-weight mannan and low-molecular-weight mannose and oligosaccharide units composed of mannose. Both types of carbohydrate are attached to the peptide. The extent of radioactive incorporation into these different carbohydrate constituents of the glycopeptide remained constant during a pulse-chase experiment. No evidence of a sequential synthesis of oligosaccharides and high-molecular-weight mannan was obtained. 4. Cycloheximide inhibits the incorporation of threonine into the wall but only partially inhibits the incorporation of glucose. Thus not all the polysaccharide deposited into the wall is dependent on a simultaneous peptide synthesis and incorporation. 5. Protoplasts grown in an iso-osmotic medium secreted a mannan polymer that was probably a glycopeptide.


1996 ◽  
Vol 7 (12) ◽  
pp. 1967-1976 ◽  
Author(s):  
S Sturm ◽  
H Okayama

In Schizosaccharomyces pombe the "start" of the cell cycle is regulated by two parallel, functionally overlapping complexes composed of Res1-Cdc10 and Res2-Cdc10. Res1 and Res2 are structurally very homologous and are required for the start of the mitotic and meiotic cycle, respectively. We have addressed the question which parts of the proteins are essential for function and determine the functional specificity. Several discrete domains in the nonconserved C-terminal region are essential for the mitotic and meiotic start function and determine the functional specificity independently of the structurally conserved motifs at the N-terminal end and in the center. One of these domains in Res2 restricts Res2 to interact only with Rep2. Res2 without this domain behaves like a functional chimera having the properties of Res2 and Res1. Likewise, internally truncated forms of Res1 lacking the centrally located ankyrin repeats and adjacent sequences can partially suppress the meiotic defect in res2- cells. These truncated Res1 molecules behave like functional chimeras with the properties of Res1 and Res2.


Author(s):  
Giulia Maria Pires dos Santos ◽  
Gustavo Ramalho Cardoso dos Santos ◽  
Mariana Ingrid Dutra da Silva Xisto ◽  
Rodrigo Rollin-Pinheiro ◽  
Andréa Regina de Souza Baptista ◽  
...  

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