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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
11

Control of cell division by nutrients, and ER stress signaling in Saccharomyces cerevisiae

Guo, Jinbai 17 September 2007 (has links)
Cell cycle progression of Saccharomyces cerevisiae cells was monitored in continuous cultures limited for glucose or nitrogen. The G1 cell cycle phase, before initiation of DNA replication, did not exclusively expand when growth rate decreased. Especially during nitrogen limitation, non-G1 phases expanded almost as much as G1. In addition, cell size remained constant as a function of growth rate. These results contrast with current views that growth requirements are met before initiation of DNA replication, and suggest that distinct nutrient limitations differentially impinge on cell cycle progression. Therefore, multiple mechanisms are hypothesized to regulate the coordination of cell growth and cell division. Genetic interactions were identified between the dose-dependent cell-cycle regulator 2 (DCR2) phosphatase and genes involving in secretion/unfolded protein response pathway, including IRE1, through a genome-wide dominant negative genetic approach. Accumulation of unfolded proteins in the endoplasmic reticulum triggers the unfolded protein response (UPR). How the UPR is downregulated is not well understood. Inositol requirement 1 (IRE1) is an endoplasmic reticulum transmembrane UPR sensor in Saccharomyces cerevisiae. When the UPR is triggered, Ire1p is autophosphorylated, on Ser 840 and Ser 841, inducing the cytosolic endonuclease activity of Ire1p, thereby initiating the splicing and translational de-repression of HAC1 mRNA. Homologous to Atf/Creb1 (Hac1p) activates UPR transcription. We found that that Dcr2p phosphatase functionally and physically interacts with Ire1p. Overexpression of DCR2, but not of a catalytically inactive DCR2 allele, significantly delays HAC1 splicing and sensitizes cells to the UPR. Furthermore, Dcr2p physically interacts in vivo with Ire1p-S840E, S841E, which mimics phosphorylated Ire1p, and Dcr2p dephosphorylates Ire1p in vitro. Our results are consistent with de-phosphorylation of Ire1p being a mechanism for antagonizing UPR signaling.
12

Control of cell division in the filamentous green alga Zygnema

Staker, Robert Dale, 1945- January 1971 (has links)
No description available.
13

Cell division in Griffithsia pacifica Kylin

Renner, Mark Edward, 1950- January 1976 (has links)
No description available.
14

Characterization of a combined DNA initiation and cell division mutant of Bacillus subtilis

Travis, Sandra Lynn, 1940- January 1975 (has links)
No description available.
15

Mitotic and chromosomal variations in a cell culture of Potorous tridactylus

Maddox, J. J. (Jimmy Joe) 08 1900 (has links)
No description available.
16

The mitotic cycle in Trillium.

MacDonald, Nancy Ruth January 1967 (has links)
No description available.
17

Cell division in the adult Drosophila brain : a clonal, bromodeoxyuridine, and ethynyl deoxyuridine analysis

Von Trotha, Jakob William January 2010 (has links)
No description available.
18

UV-induced mitotic crossing over in aspergillus.

Wood, Stephen January 1967 (has links)
No description available.
19

Role of dolichyl phosphate, N-linked glycosylation and cell membrane expression of insulin-like growth factor-1 receptor in maintenance of malignant cell growth /

Dricu, Anica, January 1900 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst. / Härtill 5 uppsatser.
20

The significance of the N-terminal region of TolQ in maintaining Tol-associated energy-dependent functions and cell division in Escherichia coli

Teleha, Mary A. January 2009 (has links)
Thesis (M.S.)--Bowling Green State University, 2009. / Document formatted into pages; contains ix, 68 p. : col. ill. Includes bibliographical references.

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