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Degradation of a-factor by a Saccharomyces cerevisiae alpha-mating-type-specific endopeptidase: evidence for a role in recovery of cells from G1 arrest.

作者信息

Marcus S, Xue C B, Naider F, Becker J M

机构信息

Department of Microbiology, University of Tennessee, Knoxville 37996.

出版信息

Mol Cell Biol. 1991 Feb;11(2):1030-9. doi: 10.1128/mcb.11.2.1030-1039.1991.

Abstract

Mating response between opposite mating types of Saccharomyces cerevisiae is dependent upon alpha factor, a tridecapeptide, and a-factor, an isoprenylated, methyl esterified dodecapeptide whose interaction with the alpha target cell has not been characterized. We report on the first biochemical and physiological evidence of an alpha-mating-type-specific a-factor-degrading activity. Radioiodinated a-factor was used to identify the a-factor-degrading activity, which is cell associated, endoproteolytic, and not required for response to pheromone. a-factor degradation was not energy dependent, nor did it require pheromone internalization or interaction with its receptor. Phenylmethylsulfonyl fluoride and tosyl-L-arginyl-methyl ester inhibited degradation of a-factor and increased the time required by alpha cells to recover from a-factor-induced growth arrest and morphological alteration, providing evidence that a-factor degradation plays a role in the recovery of alpha cells from the pheromone response.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61f/359773/fadfe3d4c970/molcellb00137-0459-a.jpg

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