Matches in SemOpenAlex for { <https://semopenalex.org/work/W2051237142> ?p ?o ?g. }
- W2051237142 endingPage "961" @default.
- W2051237142 startingPage "949" @default.
- W2051237142 abstract "The yeast a-factor receptor (encoded by STE3) is subject to two modes of endocytosis, a ligand-dependent endocytosis as well as a constitutive, ligand-independent mode. Both modes are associated with receptor ubiquitination (Roth, A.F., and N.G. Davis. 1996. J. Cell Biol. 134:661–674) and both depend on sequence elements within the receptor's regulatory, cytoplasmically disposed, COOH-terminal domain (CTD). Here, we concentrate on the Ste3p sequences required for constitutive endocytosis. Constitutive endocytosis is rapid. Receptor is synthesized, delivered to the cell surface, endocytosed, and then delivered to the vacuole where it is degraded, all with a t1/2 of 15 min. Deletion analysis has defined a 36-residue-long sequence mapping near the COOH-terminal end of the Ste3p CTD that is the minimal sequence required for this rapid turnover. Deletions intruding into this interval block or severely slow the rate of endocytic turnover. Moreover, the same 36-residue sequence directs receptor ubiquitination. Mutants deleted for this sequence show undetectable levels of ubiquitination, and mutants having intermediate endocytosis defects show a correlated reduced level of ubiquitination. Not only necessary for ubiquitination and endocytosis, this sequence also is sufficient. When transplanted to a stable cell surface protein, the plasma membrane ATPase Pma1p, the 36-residue STE3 signal directs both ubiquitination of the PMA1-STE3 fusion protein as well as its endocytosis and consequent vacuolar degradation. Alanine scanning mutagenesis across the 36-residue-long interval highlights its overall complexity—no singular sequence motif or signal is found, instead required sequence elements distribute throughout the entire interval. The high proportion of acidic and hydroxylated amino acid residues in this interval suggests a similarity to PEST sequences—a broad class of sequences which have been shown to direct the ubiquitination and subsequent proteosomal degradation of short-lived nuclear and cytoplasmic proteins. A likely possibility, therefore, is that this sequence, responsible for both endocytosis and ubiquitination, may be first and foremost a ubiquitination signal. Finally, we present evidence suggesting that the true signal in the wild-type receptor extends beyond the 36-residue-long sequence defined as a minimal signal to include contiguous PEST-like sequences which extend another 21 residues to the COOH terminus of Ste3p. Together with sequences identified in two other yeast plasma membrane proteins, the STE3 sequence defines a new class of ubiquitination/endocytosis signal." @default.
- W2051237142 created "2016-06-24" @default.
- W2051237142 creator A5021617351 @default.
- W2051237142 creator A5046275719 @default.
- W2051237142 creator A5075374436 @default.
- W2051237142 date "1998-08-24" @default.
- W2051237142 modified "2023-10-15" @default.
- W2051237142 title "A Large PEST-like Sequence Directs the Ubiquitination, Endocytosis, and Vacuolar Degradation of the Yeast a-Factor Receptor" @default.
- W2051237142 cites W1559808711 @default.
- W2051237142 cites W1571547690 @default.
- W2051237142 cites W1843483734 @default.
- W2051237142 cites W1978088045 @default.
- W2051237142 cites W1992439299 @default.
- W2051237142 cites W1996987868 @default.
- W2051237142 cites W2004281842 @default.
- W2051237142 cites W2010601153 @default.
- W2051237142 cites W2012531467 @default.
- W2051237142 cites W2024812887 @default.
- W2051237142 cites W2036110908 @default.
- W2051237142 cites W2044699962 @default.
- W2051237142 cites W2047766466 @default.
- W2051237142 cites W2052562460 @default.
- W2051237142 cites W2053632669 @default.
- W2051237142 cites W2054522434 @default.
- W2051237142 cites W2061668632 @default.
- W2051237142 cites W2063053734 @default.
- W2051237142 cites W2063190856 @default.
- W2051237142 cites W2071191421 @default.
- W2051237142 cites W20741063 @default.
- W2051237142 cites W2080273350 @default.
- W2051237142 cites W2094866737 @default.
- W2051237142 cites W2097447956 @default.
- W2051237142 cites W2098976587 @default.
- W2051237142 cites W2105451911 @default.
- W2051237142 cites W2106724679 @default.
- W2051237142 cites W2111211256 @default.
- W2051237142 cites W2118600791 @default.
- W2051237142 cites W2118848510 @default.
- W2051237142 cites W2121781216 @default.
- W2051237142 cites W2122412269 @default.
- W2051237142 cites W2124312362 @default.
- W2051237142 cites W2134344512 @default.
- W2051237142 cites W2139474586 @default.
- W2051237142 cites W2142498139 @default.
- W2051237142 cites W2164186781 @default.
- W2051237142 cites W2168196009 @default.
- W2051237142 cites W2169333620 @default.
- W2051237142 cites W2888511473 @default.
- W2051237142 cites W93114066 @default.
- W2051237142 doi "https://doi.org/10.1083/jcb.142.4.949" @default.
- W2051237142 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2132879" @default.
- W2051237142 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9722608" @default.
- W2051237142 hasPublicationYear "1998" @default.
- W2051237142 type Work @default.
- W2051237142 sameAs 2051237142 @default.
- W2051237142 citedByCount "97" @default.
- W2051237142 countsByYear W20512371422012 @default.
- W2051237142 countsByYear W20512371422013 @default.
- W2051237142 countsByYear W20512371422015 @default.
- W2051237142 countsByYear W20512371422017 @default.
- W2051237142 countsByYear W20512371422018 @default.
- W2051237142 countsByYear W20512371422019 @default.
- W2051237142 countsByYear W20512371422020 @default.
- W2051237142 countsByYear W20512371422021 @default.
- W2051237142 countsByYear W20512371422022 @default.
- W2051237142 countsByYear W20512371422023 @default.
- W2051237142 crossrefType "journal-article" @default.
- W2051237142 hasAuthorship W2051237142A5021617351 @default.
- W2051237142 hasAuthorship W2051237142A5046275719 @default.
- W2051237142 hasAuthorship W2051237142A5075374436 @default.
- W2051237142 hasBestOaLocation W20512371421 @default.
- W2051237142 hasConcept C104317684 @default.
- W2051237142 hasConcept C117943116 @default.
- W2051237142 hasConcept C143065580 @default.
- W2051237142 hasConcept C153911025 @default.
- W2051237142 hasConcept C170493617 @default.
- W2051237142 hasConcept C25602115 @default.
- W2051237142 hasConcept C28005876 @default.
- W2051237142 hasConcept C55493867 @default.
- W2051237142 hasConcept C79747257 @default.
- W2051237142 hasConcept C86803240 @default.
- W2051237142 hasConcept C95444343 @default.
- W2051237142 hasConceptScore W2051237142C104317684 @default.
- W2051237142 hasConceptScore W2051237142C117943116 @default.
- W2051237142 hasConceptScore W2051237142C143065580 @default.
- W2051237142 hasConceptScore W2051237142C153911025 @default.
- W2051237142 hasConceptScore W2051237142C170493617 @default.
- W2051237142 hasConceptScore W2051237142C25602115 @default.
- W2051237142 hasConceptScore W2051237142C28005876 @default.
- W2051237142 hasConceptScore W2051237142C55493867 @default.
- W2051237142 hasConceptScore W2051237142C79747257 @default.
- W2051237142 hasConceptScore W2051237142C86803240 @default.
- W2051237142 hasConceptScore W2051237142C95444343 @default.
- W2051237142 hasIssue "4" @default.
- W2051237142 hasLocation W20512371421 @default.
- W2051237142 hasLocation W20512371422 @default.
- W2051237142 hasLocation W20512371423 @default.
- W2051237142 hasLocation W20512371424 @default.