Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1997 Apr;8(4):647-62.
doi: 10.1091/mbc.8.4.647.

Sec3p is involved in secretion and morphogenesis in Saccharomyces cerevisiae

Affiliations
Free PMC article

Sec3p is involved in secretion and morphogenesis in Saccharomyces cerevisiae

F P Finger et al. Mol Biol Cell. 1997 Apr.
Free PMC article

Abstract

Two new temperature-sensitive alleles of SEC3, 1 of 10 late-acting SEC genes required for targeting or fusion of post-Golgi secretory vesicles to the plasma membrane in Saccharomyces cerevisiae, were isolated in a screen for temperature-sensitive secretory mutants that are synthetically lethal with sec4-8. The new sec3 alleles affect early as well as late stages of secretion. Cloning and sequencing of the SEC3 gene revealed that it is identical to profilin synthetic lethal 1 (PSL1). The SEC3 gene is not essential because cells depleted of Sec3p are viable although slow growing and temperature sensitive. All of the sec3 alleles genetically interact with a profilin mutation, pfy1-111. The SEC3 gene in high copy suppresses pfy1-111 and sec5-24 and causes synthetic growth defects with ypt1, sec8-9, sec10-2, and sec15-1. Actin structure is only perturbed in conditions of chronic loss of Sec3p function, implying that Sec3p does not directly regulate actin. All alleles of sec3 cause bud site selection defects in homozygous diploids, as do sec4-8 and sec9-4. This suggests that SEC gene products are involved in determining the bud site and is consistent with a role for Sec3p in determining the correct site of exocytosis.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Cell Biol. 1990 Jan;110(1):105-14 - PubMed
    1. Neuron. 1996 Dec;17(6):1209-19 - PubMed
    1. J Cell Biol. 1990 Jul;111(1):131-42 - PubMed
    1. J Cell Biol. 1990 Jul;111(1):143-52 - PubMed
    1. J Cell Biol. 1990 Aug;111(2):361-8 - PubMed

Publication types

MeSH terms

LinkOut - more resources