Distinct Roles for Key Karyogamy Proteins during Yeast Nuclear Fusion

被引:21
作者
Melloy, Patricia [1 ,2 ]
Shen, Shu [1 ]
White, Erin [3 ]
Rose, Mark D. [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Fairleigh Dickinson Univ, Dept Biol & Allied Hlth Sci, Madison, NJ 07940 USA
[3] Univ Colorado, MCD Biol, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
SPINDLE POLE BODY; SACCHAROMYCES-CEREVISIAE; MEMBRANE-FUSION; GENE; DOMAIN; KAR2; TRANSLOCATION; DUPLICATION; DEGRADATION; TOMOGRAPHY;
D O I
10.1091/mbc.E09-02-0163
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
During yeast mating, cell fusion is followed by the congression and fusion of the two nuclei. Proteins required for nuclear fusion are found at the surface (Prm3p) and within the lumen (Kar2p, Kar5p, and Kar8p) of the nuclear envelope (NE). Electron tomography (ET) of zygotes revealed that mutations in these proteins block nuclear fusion with different morphologies, suggesting that they act in different steps of fusion. Specifically, prm3 zygotes were blocked before formation of membrane bridges, whereas kar2, kar5, and kar8 zygotes frequently contained them. Membrane bridges were significantly larger and occurred more frequently in kar2 and kar8, than in kar5 mutant zygotes. The kinetics of NE fusion in prm3, kar5, and kar8 mutants, measured by live-cell fluorescence microscopy, were well correlated with the size and frequency of bridges observed by ET. However the kar2 mutant was defective for transfer of NE lumenal GFP, but not diffusion within the lumen, suggesting that transfer was blocked at the NE fusion junction. These observations suggest that Prm3p acts before initiation of outer NE fusion, Kar5p may help dilation of the initial fusion pore, and Kar2p and Kar8p act after outer NE fusion, during inner NE fusion.
引用
收藏
页码:3773 / 3782
页数:10
相关论文
共 35 条
[1]
Amberg D. C., 2005, METHODS YEAST GENETI
[2]
A walk-through of the yeast mating pheromone response pathway (vol 25, pg 1465, 2004) [J].
Bardwell, L .
PEPTIDES, 2005, 26 (02) :337-+
[3]
KAR5 encodes a novel pheromone-inducible protein required for homotypic nuclear fusion [J].
Beh, CT ;
Brizzio, V ;
Rose, MD .
JOURNAL OF CELL BIOLOGY, 1997, 139 (05) :1063-1076
[4]
Bipartite signals mediate subcellular targeting of tail-anchored membrane proteins in Saccharomyces cerevisiae [J].
Beilharz, T ;
Egan, B ;
Silver, PA ;
Hofmann, K ;
Lithgow, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (10) :8219-8223
[5]
Genetic interactions between KAR7/SEC71, KAR8/JEM1, KAR5, and KAR2 during nuclear fusion in Saccharomyces cerevisiae [J].
Brizzio, V ;
Khalfan, W ;
Huddler, D ;
Beh, CT ;
Andersen, SSL ;
Latterich, M ;
Rose, MD .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (03) :609-626
[6]
Pheromone response, mating and cell biology [J].
Elion, EA .
CURRENT OPINION IN MICROBIOLOGY, 2000, 3 (06) :573-581
[7]
Pheromone-regulated genes required for yeast mating differentiation [J].
Erdman, S ;
Lin, L ;
Malczynski, M ;
Snyder, M .
JOURNAL OF CELL BIOLOGY, 1998, 140 (03) :461-483
[8]
Gammie AE, 2002, METHOD ENZYMOL, V351, P477
[9]
Prm1p, a pheromone-regulated multispanning membrane protein, facilitates plasma membrane fusion during yeast mating [J].
Heiman, MG ;
Walter, P .
JOURNAL OF CELL BIOLOGY, 2000, 151 (03) :719-730
[10]
The budding yeast spindle pole body: Structure, duplication, and function [J].
Jaspersen, SL ;
Winey, M .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2004, 20 :1-28