Co-regulation of polar mRNA transport and lifespan in budding yeast Saccharomyces cerevisiae

被引:3
作者
Taranukha, Dmitri [1 ,3 ]
Budovsky, Arie [1 ]
Gobshtis, Nikolai [1 ,3 ]
Braiman, Alex [1 ]
Porat, Ziv [2 ]
Aronov, Stella [3 ]
Fraifeld, Vadim E. [1 ]
机构
[1] Ben Gurion Univ Negev, Ctr Multidisciplinary Res Aging, Shraga Segal Dept Microbiol Immunol & Genet, IL-84105 Beer Sheva, Israel
[2] Weizmann Inst Sci, Flow Cytometry Unit, IL-76100 Rehovot, Israel
[3] Ariel Univ, Ctr Samaria, Dept Mol Biol, Ariel, Israel
关键词
yeast; lifespan; longevity genes; cell polarity; granules; P-bodies; mRNA transport; ImageStreamX; P-BODIES; MESENCHYMAL TRANSITION; CELLS; TRANSLATION; MECHANISM; GROWTH; BUD; SEGREGATION; STRESS;
D O I
10.4161/cc.22659
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent studies have uncovered the links between aging, rejuvenation and polar protein transport in the budding yeast Saccharomyces cerevisiae. Here, we examined a still unexplored possibility for co-regulation of polar mRNA transport and lifespan. To monitor the amount and distribution of mRNA-containing granules in mother and daughter cells, we used a fluorescent mRNA-labeling system, with MFA2 as a reporter gene. The results obtained showed that deletion of the selected longevity regulators in budding yeast had a significant impact on the polar mRNA transport. This included changes in the amount of mRNA-containing granules in cytoplasm, their aggregation and distribution between the mother and daughter cells. A significant negative correlation was found between strain-specific longevity, amount of granules and total fluorescent intensity both in mother and daughter cells. As indicated by the coefficient of determination, approximately 50-75% of variation in yeast lifespan could be attributed to the differences in polar mRNA transport.
引用
收藏
页码:4275 / 4280
页数:6
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