Analýza mutantů Rpg1/eIF3a v Saccharomyces cerevisiae.

Rpg1/Tif32/eIF3a is an essential and the largest subunit of translation initiation factor eIF3 in yeast Saccharomyces cerevisiae. Besides interactions within the eIF3 complex it has been shown to interact with microtubules. Preliminary data of the laboratory obtained using strains of the W303 geneti...

Full description

Bibliographic Details
Main Author: Luxová, Pavla
Other Authors: Malcová, Ivana
Format: Dissertation
Language:Czech
Published: 2014
Online Access:http://www.nusl.cz/ntk/nusl-337642
Description
Summary:Rpg1/Tif32/eIF3a is an essential and the largest subunit of translation initiation factor eIF3 in yeast Saccharomyces cerevisiae. Besides interactions within the eIF3 complex it has been shown to interact with microtubules. Preliminary data of the laboratory obtained using strains of the W303 genetic background indicated that there is a synthetic phenotype between rpg1-2 mutant and microtubule inhibitor nocodazole. Aim of this work to elucidate this "microtubule phenotype" of the rpg1-2 mutant and its dependency on used genetic background. I confirmed that independently on genetic background (W303, BY, SEY) all mutants rpg1-1, rpg1-2 and rpg1-3 were temperature- sensitive. I found that in contrast to published data on rpg1 mutants of the W303 background these mutants of the BY and the SEY backgrounds do not arrest the cell cycle in G1 phase during cultivation at the restrictive temperature (37řC, 4 hours). In addition, all three mutants did not show an increased sensitivity to benomyl and none of them affects microtubule rearrangement after a release of cells from the nocodazole treatment. I constructed new strains with a combination of the BUB1 gene deletion with the particular rpg1 mutation. Phenotypic analyses of new double mutants revealed that simultaneous dis-function of Bub1 and Rpg1 results...