Matches in SemOpenAlex for { <https://semopenalex.org/work/W2118861729> ?p ?o ?g. }
- W2118861729 endingPage "136" @default.
- W2118861729 startingPage "125" @default.
- W2118861729 abstract "Two different mutations in the arginine vasopressin (AVP) gene associated with autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) predict Y21H (AVP2) and V67A (NP36) amino acid substitutions of the AVP prohormone. They are unique in that they change, respectively, the AVP moiety and a region of the neurophysin II domain not so far affected by any mutations. To test whether they affect the cellular handling of the AVP prohormone in a similar manner to previously investigated mutations, they were examined by heterologous expression in cell lines.Both mutations resulted in significantly reduced amounts of immunoreactive AVP in the cell culture medium as determined by radioimmunoassay analysis. Metabolic labelling combined with immunoprecipitation demonstrated that processing and secretion of the mutant prohormones was reduced but not prevented. Finally, confocal laser scanning microscopy showed that normal AVP prohormone and/or its processed products were localized in the tips of the cellular processes, whereas both mutant prohormones were accumulated in the endoplasmic reticulum (ER) and in the case of the V67A prohormone, also in perinuclear structures outside the ER.Both mutations result in reduced AVP prohormone processing and secretion probably due to retention in the ER. This supports, at least partly, the hypothesis that the mutations lead to the production of a mutant hormone precursor that fails to fold and/or dimerize properly and, as a consequence, is retained by the ER protein quality control machinery. Perinuclear accumulation of the V67A prohormone outside the ER indicates that additional mechanisms could be involved." @default.
- W2118861729 created "2016-06-24" @default.
- W2118861729 creator A5005874091 @default.
- W2118861729 creator A5011371299 @default.
- W2118861729 creator A5041703724 @default.
- W2118861729 creator A5046382012 @default.
- W2118861729 creator A5079656816 @default.
- W2118861729 creator A5087819197 @default.
- W2118861729 creator A5088063367 @default.
- W2118861729 date "2003-12-17" @default.
- W2118861729 modified "2023-10-14" @default.
- W2118861729 title "Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus" @default.
- W2118861729 cites W1508709878 @default.
- W2118861729 cites W1592910316 @default.
- W2118861729 cites W1775749144 @default.
- W2118861729 cites W1966207769 @default.
- W2118861729 cites W1968032473 @default.
- W2118861729 cites W1974283924 @default.
- W2118861729 cites W1976018037 @default.
- W2118861729 cites W1978307712 @default.
- W2118861729 cites W1986129246 @default.
- W2118861729 cites W1986497103 @default.
- W2118861729 cites W1988146888 @default.
- W2118861729 cites W1999347864 @default.
- W2118861729 cites W2007852891 @default.
- W2118861729 cites W2010011508 @default.
- W2118861729 cites W2020815069 @default.
- W2118861729 cites W2045463547 @default.
- W2118861729 cites W2045893780 @default.
- W2118861729 cites W2047000276 @default.
- W2118861729 cites W2048117183 @default.
- W2118861729 cites W2048592634 @default.
- W2118861729 cites W2053349628 @default.
- W2118861729 cites W2072917593 @default.
- W2118861729 cites W2080908359 @default.
- W2118861729 cites W2087662274 @default.
- W2118861729 cites W2096042446 @default.
- W2118861729 cites W2106001283 @default.
- W2118861729 cites W2111250434 @default.
- W2118861729 cites W2118350579 @default.
- W2118861729 cites W2120653693 @default.
- W2118861729 cites W2127570644 @default.
- W2118861729 cites W2149761960 @default.
- W2118861729 cites W2164065816 @default.
- W2118861729 cites W2165136392 @default.
- W2118861729 cites W2185681687 @default.
- W2118861729 cites W4236547687 @default.
- W2118861729 cites W4236660413 @default.
- W2118861729 cites W4236836821 @default.
- W2118861729 cites W4241492121 @default.
- W2118861729 cites W4244269474 @default.
- W2118861729 cites W4248333976 @default.
- W2118861729 doi "https://doi.org/10.1111/j.1365-2265.2004.01953.x" @default.
- W2118861729 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14678298" @default.
- W2118861729 hasPublicationYear "2003" @default.
- W2118861729 type Work @default.
- W2118861729 sameAs 2118861729 @default.
- W2118861729 citedByCount "34" @default.
- W2118861729 countsByYear W21188617292012 @default.
- W2118861729 countsByYear W21188617292013 @default.
- W2118861729 countsByYear W21188617292015 @default.
- W2118861729 countsByYear W21188617292016 @default.
- W2118861729 countsByYear W21188617292017 @default.
- W2118861729 countsByYear W21188617292018 @default.
- W2118861729 countsByYear W21188617292019 @default.
- W2118861729 countsByYear W21188617292021 @default.
- W2118861729 countsByYear W21188617292022 @default.
- W2118861729 crossrefType "journal-article" @default.
- W2118861729 hasAuthorship W2118861729A5005874091 @default.
- W2118861729 hasAuthorship W2118861729A5011371299 @default.
- W2118861729 hasAuthorship W2118861729A5041703724 @default.
- W2118861729 hasAuthorship W2118861729A5046382012 @default.
- W2118861729 hasAuthorship W2118861729A5079656816 @default.
- W2118861729 hasAuthorship W2118861729A5087819197 @default.
- W2118861729 hasAuthorship W2118861729A5088063367 @default.
- W2118861729 hasConcept C104317684 @default.
- W2118861729 hasConcept C126322002 @default.
- W2118861729 hasConcept C134018914 @default.
- W2118861729 hasConcept C143065580 @default.
- W2118861729 hasConcept C158617107 @default.
- W2118861729 hasConcept C2776370428 @default.
- W2118861729 hasConcept C2776958162 @default.
- W2118861729 hasConcept C2777468819 @default.
- W2118861729 hasConcept C2780090379 @default.
- W2118861729 hasConcept C515207424 @default.
- W2118861729 hasConcept C55493867 @default.
- W2118861729 hasConcept C71315377 @default.
- W2118861729 hasConcept C71924100 @default.
- W2118861729 hasConcept C86803240 @default.
- W2118861729 hasConcept C95444343 @default.
- W2118861729 hasConceptScore W2118861729C104317684 @default.
- W2118861729 hasConceptScore W2118861729C126322002 @default.
- W2118861729 hasConceptScore W2118861729C134018914 @default.
- W2118861729 hasConceptScore W2118861729C143065580 @default.
- W2118861729 hasConceptScore W2118861729C158617107 @default.
- W2118861729 hasConceptScore W2118861729C2776370428 @default.
- W2118861729 hasConceptScore W2118861729C2776958162 @default.
- W2118861729 hasConceptScore W2118861729C2777468819 @default.