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Conjugation rescue of an exocytosis-competent membrane microdomain in Tetrahymena thermophila mutants.

作者信息

Satir B H, Reichman M, Orias E

出版信息

Proc Natl Acad Sci U S A. 1986 Nov;83(21):8221-5. doi: 10.1073/pnas.83.21.8221.

DOI:10.1073/pnas.83.21.8221
PMID:3464949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC386899/
Abstract

Conjugation-rescue experiments with two Tetrahymena thermophila mutants (exo-) incapable of exocytosis (SB255, SB258) have been used to dissect regulatory steps in assembly of a functional membrane microdomain, the fusion rosette. "Rescue" refers to the recovery of a secretory activity. Exo- mutants fail to secrete mucus normally (form capsules) when stimulated by the secretagogue alcian blue and are blocked before the assembly of a functional fusion rosette in the cell membrane. Two criteria are used to assay recovery of the wild-type (exo+) phenotype: the conjugant's ability to form capsules when stimulated and the presence of assembled rosettes, which disperse upon stimulation. Conjugation of exo+ X SB258 results in restoration of secretion in 60% of the mutant conjugants and reappearance of assembled rosettes. Secretory capacity is restored in the SB258 cell within one-half hour of firm pair formation. This restoration is not due to new gene expression or continued protein synthesis, since it occurs when SB258 is crossed to a "star" strain (A*), which has defective micronuclei and therefore cannot contribute wild-type genes, and restoration occurs in the presence of cycloheximide during conjugation. Conjugation of exo+ X SB255 reveals a real but inefficient restoration of exocytic capacity in the exo- conjugant and a significant decrease of exocytic capacity in the exo+ conjugant. SB255 X SB258 crosses also show a low but significant rescue of exocytic competence, indicating that different components of the exocytic mechanism are affected in the two mutants. This cross leads to restoration of rosette assembly and function in one of the partners, presumably SB258. These results provide data about some of the steps necessary for rosette assembly and suggest that transferable factors that promote and/or inhibit exocytosis are present in these cells.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c869/386899/ee3585444fe2/pnas00325-0213-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c869/386899/ee3585444fe2/pnas00325-0213-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c869/386899/ee3585444fe2/pnas00325-0213-a.jpg

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本文引用的文献

1
Restoration of membrane excitability in a behavioral mutant of Paramecium caudatum during conjugation and by microinjection of wild-type cytoplasm.尾草履虫行为突变体在接合过程中及通过显微注射野生型细胞质恢复膜兴奋性。
J Cell Biol. 1980 Feb;84(2):476-80. doi: 10.1083/jcb.84.2.476.
2
Control of exocytotic processes: cytological and physiological studies of trichocyst mutants in Paramecium tetraurelia.胞吐过程的调控:四膜虫中刺丝泡突变体的细胞学与生理学研究
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Conjugation in Tetrahymena thermophila. A temporal analysis of cytological stages.
颗粒晶格蛋白1(Grl1p)是嗜热四膜虫致密核心分泌颗粒中的一种酸性钙结合蛋白,它影响颗粒的大小、形状、内容物组织和释放,但不影响蛋白质分选或凝聚。
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Maturation of dense core granules in wild type and mutant Tetrahymena thermophila.野生型和突变型嗜热四膜虫中致密核心颗粒的成熟
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Isolation and ultrastructural characterization of secretory mutants of Tetrahymena thermophila.嗜热四膜虫分泌突变体的分离与超微结构表征
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Cytogenetics of genomic exclusion in Tetrahymena.四膜虫基因组排除的细胞遗传学
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6
Membrane fusion in a model system. Mucocyst secretion in Tetrahymena.模型系统中的膜融合。四膜虫中的黏液囊泡分泌。
J Cell Biol. 1973 Jan;56(1):153-76. doi: 10.1083/jcb.56.1.153.
7
Membrane reorganization during secretion in Tetrahymena.四膜虫分泌过程中的膜重组。
Nature. 1972 Jan 7;235(5332):53-4. doi: 10.1038/235053a0.
8
Pair formation in tetrahymena pyriformis, an inducible developmental system.梨形四膜虫中的配对形成,一种可诱导的发育系统。
J Exp Zool. 1974 Jun;188(3):337-44. doi: 10.1002/jez.1401880309.
9
Protein secretion in Tetrahymena thermophila: characterization of the secretory mutant strain SB281.
J Cell Sci. 1985 Oct;78:49-65. doi: 10.1242/jcs.78.1.49.
10
Gene expression and phenotypic change in Paramecium tetraurelia exconjugants.四膜虫接合后体中的基因表达与表型变化。
Genet Res. 1976 Apr;27(2):123-34. doi: 10.1017/s0016672300016335.