Matches in SemOpenAlex for { <https://semopenalex.org/work/W2095321176> ?p ?o ?g. }
- W2095321176 endingPage "235" @default.
- W2095321176 startingPage "230" @default.
- W2095321176 abstract "<h3>Background</h3> Ostium secundum atrial septal defects (ASDII) account for approximately 10% of all congenital heart defects (CHD), and mutations in cardiac transcription factors, including <i>TBX20</i>, were identified as an underlying cause for ASDII. However, very little is known about disease penetrance in families and functional consequences of inherited TBX20 mutations. <h3>Methods</h3> The coding region of <i>TBX20</i> was directly sequenced in 170 ASDII patients. Functional consequences of one novel mutation were investigated by surface plasmon resonance, CD spectropolarymetry, fluorescence spectrophotometry, luciferase assay and chromatin immunoprecipitation. <h3>Results</h3> We found a novel mutation in a highly conserved residue in the T-box DNA binding domain (I121M) segregating with CHD in a three generation kindred. Four mutation carriers revealed cardiac phenotypes in terms of cribriform ASDII, large patent foramen ovale or cardiac valve defects. Interestingly, tertiary hydrophobic interactions within the mutant TBX20 T-box were significantly altered leading to a more dynamic structure of the protein. Moreover, Tbx20-I121M resulted in a significantly enhanced transcriptional activity, which was further increased in the presence of co-transcription factors GATA4/5 and NKX2-5. Occupancy of DNA binding sites on target genes was also increased. <h3>Conclusions</h3> We suggest that TBX20-I121M adopts a more fluid tertiary structure leading to enhanced interactions with cofactors and more stable transcriptional complexes on target DNA sequences. Our data, combined with that of others, suggest that human ASDII may be related to loss-of-function as well as gain-of-function TBX20 mutations." @default.
- W2095321176 created "2016-06-24" @default.
- W2095321176 creator A5005384946 @default.
- W2095321176 creator A5018441388 @default.
- W2095321176 creator A5023586883 @default.
- W2095321176 creator A5024422486 @default.
- W2095321176 creator A5028804707 @default.
- W2095321176 creator A5031654956 @default.
- W2095321176 creator A5037320109 @default.
- W2095321176 creator A5044362390 @default.
- W2095321176 creator A5051229043 @default.
- W2095321176 creator A5054308820 @default.
- W2095321176 creator A5058135387 @default.
- W2095321176 creator A5059742542 @default.
- W2095321176 creator A5061874736 @default.
- W2095321176 creator A5079596222 @default.
- W2095321176 creator A5079973263 @default.
- W2095321176 creator A5083550145 @default.
- W2095321176 creator A5089377331 @default.
- W2095321176 date "2009-09-16" @default.
- W2095321176 modified "2023-10-18" @default.
- W2095321176 title "A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects" @default.
- W2095321176 cites W1989457690 @default.
- W2095321176 cites W1990240283 @default.
- W2095321176 cites W1994134406 @default.
- W2095321176 cites W2008762833 @default.
- W2095321176 cites W2010390017 @default.
- W2095321176 cites W2014510586 @default.
- W2095321176 cites W2019136158 @default.
- W2095321176 cites W2020673317 @default.
- W2095321176 cites W2023538745 @default.
- W2095321176 cites W2027058574 @default.
- W2095321176 cites W2033871452 @default.
- W2095321176 cites W2040403266 @default.
- W2095321176 cites W2040986139 @default.
- W2095321176 cites W2045998016 @default.
- W2095321176 cites W2046012351 @default.
- W2095321176 cites W2061884629 @default.
- W2095321176 cites W2097836010 @default.
- W2095321176 cites W2108285904 @default.
- W2095321176 cites W2109372707 @default.
- W2095321176 cites W2116518429 @default.
- W2095321176 cites W2120018988 @default.
- W2095321176 cites W2127387556 @default.
- W2095321176 cites W2142329485 @default.
- W2095321176 cites W2151720801 @default.
- W2095321176 cites W2157304951 @default.
- W2095321176 cites W2164004777 @default.
- W2095321176 doi "https://doi.org/10.1136/jmg.2009.069997" @default.
- W2095321176 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2981023" @default.
- W2095321176 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19762328" @default.
- W2095321176 hasPublicationYear "2009" @default.
- W2095321176 type Work @default.
- W2095321176 sameAs 2095321176 @default.
- W2095321176 citedByCount "102" @default.
- W2095321176 countsByYear W20953211762012 @default.
- W2095321176 countsByYear W20953211762013 @default.
- W2095321176 countsByYear W20953211762014 @default.
- W2095321176 countsByYear W20953211762015 @default.
- W2095321176 countsByYear W20953211762016 @default.
- W2095321176 countsByYear W20953211762017 @default.
- W2095321176 countsByYear W20953211762018 @default.
- W2095321176 countsByYear W20953211762019 @default.
- W2095321176 countsByYear W20953211762020 @default.
- W2095321176 countsByYear W20953211762021 @default.
- W2095321176 countsByYear W20953211762022 @default.
- W2095321176 countsByYear W20953211762023 @default.
- W2095321176 crossrefType "journal-article" @default.
- W2095321176 hasAuthorship W2095321176A5005384946 @default.
- W2095321176 hasAuthorship W2095321176A5018441388 @default.
- W2095321176 hasAuthorship W2095321176A5023586883 @default.
- W2095321176 hasAuthorship W2095321176A5024422486 @default.
- W2095321176 hasAuthorship W2095321176A5028804707 @default.
- W2095321176 hasAuthorship W2095321176A5031654956 @default.
- W2095321176 hasAuthorship W2095321176A5037320109 @default.
- W2095321176 hasAuthorship W2095321176A5044362390 @default.
- W2095321176 hasAuthorship W2095321176A5051229043 @default.
- W2095321176 hasAuthorship W2095321176A5054308820 @default.
- W2095321176 hasAuthorship W2095321176A5058135387 @default.
- W2095321176 hasAuthorship W2095321176A5059742542 @default.
- W2095321176 hasAuthorship W2095321176A5061874736 @default.
- W2095321176 hasAuthorship W2095321176A5079596222 @default.
- W2095321176 hasAuthorship W2095321176A5079973263 @default.
- W2095321176 hasAuthorship W2095321176A5083550145 @default.
- W2095321176 hasAuthorship W2095321176A5089377331 @default.
- W2095321176 hasBestOaLocation W20953211761 @default.
- W2095321176 hasConcept C104317684 @default.
- W2095321176 hasConcept C116186050 @default.
- W2095321176 hasConcept C501734568 @default.
- W2095321176 hasConcept C54355233 @default.
- W2095321176 hasConcept C75563809 @default.
- W2095321176 hasConcept C86339819 @default.
- W2095321176 hasConcept C86803240 @default.
- W2095321176 hasConceptScore W2095321176C104317684 @default.
- W2095321176 hasConceptScore W2095321176C116186050 @default.
- W2095321176 hasConceptScore W2095321176C501734568 @default.
- W2095321176 hasConceptScore W2095321176C54355233 @default.
- W2095321176 hasConceptScore W2095321176C75563809 @default.