Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Schizosaccharomyces pombe Proteins/genetics"'
Autor:
Ingrid Billault-Chaumartin, Laetitia Michon, Caitlin A. Anderson, Sarah E. Yde, Cristian Suarez, Justyna Iwaszkiewicz, Vincent Zoete, David R. Kovar, Sophie G. Martin
Publikováno v:
Journal of cell science, vol. 135, no. 13, pp. jcs260289
In formin-family proteins, actin filament nucleation and elongation activities reside in the formin homology 1 (FH1) and FH2 domains, with reaction rates that vary by at least 20-fold between formins. Each cell expresses distinct formins that assembl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::223cfd741e0dfbac9e37bc4508aed3a7
https://serval.unil.ch/notice/serval:BIB_3B4B0AEC5924
https://serval.unil.ch/notice/serval:BIB_3B4B0AEC5924
Publikováno v:
Current biology, vol. 32, no. 21, pp. 4752-4761.e10
bioRxiv
BioRxiv
bioRxiv
BioRxiv
Secretory vesicle clusters transported on actin filaments by myosin V motors for local secretion underlie various cellular processes, such as neurotransmitter release at neuronal synapses, 1 hyphal steering in filamentous fungi, 2 , 3 and local cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfd0d1bbe7438bd479da8553c613d8c7
https://doi.org/10.1101/2022.05.05.490810
https://doi.org/10.1101/2022.05.05.490810
Differential GAP requirement for Cdc42-GTP polarization during proliferation and sexual reproduction
Autor:
Sophie G. Martin, Daniela Gallo Castro
Publikováno v:
The Journal of Cell Biology
The Journal of cell biology, vol. 217, no. 12, pp. 4215-4229
The Journal of cell biology, vol. 217, no. 12, pp. 4215-4229
Local activity of the small GTPase Cdc42 is critical for cell polarization. Gallo Castro and Martin describe a new Cdc42 GTPase-activating protein (GAP) Rga3, which together with two other GAPs, constrains Cdc42-GTP zones during mitotic cycles but no
Publikováno v:
PLoS biology, vol. 18, no. 1, pp. e3000600
PLoS Biology, Vol 18, Iss 1, p e3000600 (2020)
PLoS Biology
PLoS Biology, Vol 18, Iss 1, p e3000600 (2020)
PLoS Biology
Local activity of the small GTPase Cdc42 is critical for cell polarization. Whereas scaffold-mediated positive feedback was proposed to break symmetry of budding yeast cells and produce a single zone of Cdc42 activity, the existence of similar regula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::545d82465c5c718399779415d9725133
Publikováno v:
Current Biology
Current biology, vol. 29, no. 19, pp. 3165-3176.e6
Current biology, vol. 29, no. 19, pp. 3165-3176.e6
Summary How actin structures of distinct identities and functions coexist within the same environment is a critical self-organization question. Fission yeast cells have a simple actin cytoskeleton made of four structures: Arp2/3 assembles actin patch
Autor:
Valérie Migeot, Marc Descrimes, Mayuko Yoda, Maxime Wery, Damien Hermand, Camille Gautier, Antonin Morillon
Publikováno v:
PLoS Genetics
PLoS Genetics, Public Library of Science, 2018, 14 (7), pp.e1007465. ⟨10.1371/journal.pgen.1007465⟩
Wery, M, Gautier, C, Descrimes, M, Yoda, M, Migeot, V, Hermand, D & Morillon, A 2018, ' Bases of antisense lncRNA-associated regulation of gene expression in fission yeast ', PLoS Genetics, vol. 14, no. 7, e1007465, pp. e1007465 . https://doi.org/10.1371/journal.pgen.1007465
PLoS Genetics, Vol 14, Iss 7, p e1007465 (2018)
PLoS Genetics, Public Library of Science, 2018, 14 (7), pp.e1007465. ⟨10.1371/journal.pgen.1007465⟩
Wery, M, Gautier, C, Descrimes, M, Yoda, M, Migeot, V, Hermand, D & Morillon, A 2018, ' Bases of antisense lncRNA-associated regulation of gene expression in fission yeast ', PLoS Genetics, vol. 14, no. 7, e1007465, pp. e1007465 . https://doi.org/10.1371/journal.pgen.1007465
PLoS Genetics, Vol 14, Iss 7, p e1007465 (2018)
Antisense (as)lncRNAs can regulate gene expression but the underlying mechanisms and the different cofactors involved remain unclear. Using Native Elongating Transcript sequencing, here we show that stabilization of antisense Exo2-sensitivite lncRNAs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb39484308f0058e70f475aa27b83419
https://hal.archives-ouvertes.fr/hal-02349807/document
https://hal.archives-ouvertes.fr/hal-02349807/document
Autor:
Kajitani, T., Kato, H., Chikashige, Y., Tsutsumi, C., Hiraoka, Y., Kimura, Hiroshi, Ohkawa, Y., Obuse, C., Hermand, D., Murakami, Y.
Publikováno v:
Kajitani, T, Kato, H, Chikashige, Y, Tsutsumi, C, Hiraoka, Y, Kimura, H, Ohkawa, Y, Obuse, C, Hermand, D & Murakami, Y 2017, ' Ser7 of RNAPII-CTD facilitates heterochromatin formation by linking ncRNA to RNAi ', Proceedings of the National Academy of Sciences of the United States of America, vol. 114, no. 52, pp. E11208-E11217 . https://doi.org/10.1073/pnas.1714579115
Some long noncoding RNAs (ncRNAs) transcribed by RNA polymerase II (RNAPII) are retained on chromatin, where they regulate RNAi and chromatin structure. The molecular basis of this retention remains unknown. We show that in fission yeast serine 7 (Se
Autor:
Bita Khalili, Laura Merlini, Omaya Dudin, Sophie G. Martin, Laetitia Michon, Vincent Vincenzetti
Publikováno v:
The Journal of Cell Biology
The Journal of cell biology, vol. 217, no. 4, pp. 1467-1483
The Journal of cell biology, vol. 217, no. 4, pp. 1467-1483
The yeast cell wall is digested to allow cell fusion during sexual reproduction. How cells coordinate this process with cell–cell contact to prevent lysis is unclear. Merlini et al. show that the Ras GAP protein Gap1, which is recruited to sites of
Autor:
Ruan, K., Yamamoto, T. G., Asakawa, H., Chikashige, Y., Kimura, Hiroshi, Masukata, H., Haraguchi, T., Hiraoka, Y.
Publikováno v:
Scientific Reports
Faithful DNA replication is a prerequisite for cell proliferation. Several cytological studies have shown that chromosome structures alter in the S-phase of the cell cycle. However, the molecular mechanisms behind the alteration of chromosome structu
Publikováno v:
Yeast, 22 (13
The ease of construction of multiple mutant strains in Schizosaccharomyces pombe is limited by the number of available genetic markers. We describe here three new cassettes for PCR-mediated gene disruption that can be used in combination with commonl