نتایج جستجو برای: fission yeast

تعداد نتایج: 98162  

2009
Domenica Paparatto Dane Fletcher Karen Piwowar Kimberly Baldino Charlotte Morel Stephen Dunaway

BACKGROUND DNA damage checkpoints insure that the integrity of genomic DNA is faithfully maintained throughout the eukaryotic cell cycle. In the presence of damaged DNA, checkpoints are triggered to delay cell cycle progression to allow for DNA repair. In fission yeast, the kinases Chk1 and Cds1 are major components of these DNA damage checkpoint pathways. Both Chk1 and Cds1 are important for v...

Journal: :The Journal of biological chemistry 2001
M Uchiyama D Griffiths K Arai H Masai

Assembly of replication complexes at the replication origins is strictly regulated. Cdc45p is known to be a part of the active replication complexes. In Xenopus egg extracts, Cdc45p was shown to be required for loading of DNA polymerase alpha onto chromatin. The fission yeast cdc45 homologue was identified as a suppressor for nda4 and named sna41. Nevertheless, it is not known how Cdc45p facili...

Journal: :Nucleic acids research 1994
David Selinger Patrick Brennwald Steven Althoff Claudia Reich Byron Hann Peter Walter Jo Ann Wise

Mammalian signal recognition particle (SRP), a complex of six polypeptides and one 7SL RNA molecule, is required for targeting nascent presecretory proteins to the endoplasmic reticulum (ER). Earlier work identified a Schizosaccharomyces pombe homolog of human SRP RNA and showed that it is a component of a particle similar in size and biochemical properties to mammalian SRP. The recent cloning ...

2015
Weronika E. Borek Juan Zou Juri Rappsilber Kenneth E. Sawin Janet F. Partridge

The use of "heavy" isotope-labeled arginine for stable isotope labeling by amino acids in cell culture (SILAC) mass spectrometry in the fission yeast Schizosaccharomyces pombe is hindered by the fact that under normal conditions, arginine is extensively catabolized in vivo, resulting in the appearance of "heavy"-isotope label in several other amino acids, most notably proline, but also glutamat...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Yan Zhang David C Chan

Mitochondrial fission controls mitochondrial shape and physiology, including mitochondrial remodeling in apoptosis. During assembly of the yeast mitochondrial fission complex, the outer membrane protein Fis1 recruits the dynamin-related GTPase Dnm1 to mitochondria. Fis1 contains a tetratricopeptide repeat (TPR) domain and interacts with Dnm1 via the molecular adaptors Mdv1 and Caf4. By using cr...

Journal: :Current Biology 2009
Brian G. Fuller P. Todd Stukenberg

Studies in fission and budding yeast have continuously led the way for analyzing pathways of cell division. Two elegant studies, one from each yeast species, are opening the gates to study one of the final steps of mitosis--silencing the spindle checkpoint.

Journal: :Current Biology 2002
Susanne Trautmann Dannel McCollum

The Cdc14 phosphatase was identified by its requirement for mitotic exit in budding yeast. Cdc14 homologs exist throughout the eukaryotic kingdom, but it was unclear whether their function would also be conserved. Recent analyses in fission yeast, humans and now C. elegans suggest numerous other functions for this family of proteins.

Journal: :Comparative and Functional Genomics 2002
Jo Wixon

Schizosaccharomyces pombe, the fission yeast, has long been a crucial model for the study of the eukaryote cell cycle. We take a look at this important yeast, whose genome has recently been completed, featuring comments from Valerie Wood, Jürg Bähler, Ramsay McFarlane, Susan Forsburg, Iain Hagan and Paul Nurse on the implications of having the complete sequence and future prospects for pombe ge...

Journal: :Current Biology 2003
Alison Pidoux Robin Allshire

Chromosome segregation depends on proper orientation of sister kinetochores. The protein Csm1 is required for mono-orientation of sister kinetochores at meiosis I in budding yeast. Surprisingly, its homologue in fission yeast appears instead of clamp micro-tubule binding sites together on single mitotic kinetochores so that they all face one spindle pole.

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