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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
1999-5-20
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pubmed:databankReference |
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pubmed:abstractText |
To better understand the role of TBX5, a T-box containing transcription factor in forelimb and heart development, we have studied the clinical features of Holt-Oram syndrome caused by 10 different TBX5 mutations. Defects predicted to create null alleles caused substantial abnormalities both in limb and heart. In contrast, missense mutations produced distinct phenotypes: Gly80Arg caused significant cardiac malformations but only minor skeletal abnormalities; and Arg237Gln and Arg237Trp caused extensive upper limb malformations but less significant cardiac abnormalities. Amino acids altered by missense mutations were located on the three-dimensional structure of a related T-box transcription factor, Xbra, bound to DNA. Residue 80 is highly conserved within T-box sequences that interact with the major groove of target DNA; residue 237 is located in the T-box domain that selectively binds to the minor groove of DNA. These structural data, taken together with the predominant cardiac or skeletal phenotype produced by each missense mutation, suggest that organ-specific gene activation by TBX5 is predicated on biophysical interactions with different target DNA sequences.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-1277635,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-14402857,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-1870097,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-1996196,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-2785681,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-480027,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-5410358,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-5904863,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-7588606,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-7623830,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-7867169,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-7920656,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8114858,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8344258,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8404501,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8575328,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8635257,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8878690,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8988164,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-8988165,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-9207801,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-9276934,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-9309177,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-9337389,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-9349824,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-9367427,
http://linkedlifedata.com/resource/pubmed/commentcorrection/10077612-9395282
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0027-8424
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pubmed:author |
pubmed-author:BachinskyD RDR,
pubmed-author:BassonC TCT,
pubmed-author:BruzzoneRR,
pubmed-author:HuangTT,
pubmed-author:KamisagoMM,
pubmed-author:KriegerJJ,
pubmed-author:LeroneMM,
pubmed-author:LinR CRC,
pubmed-author:MüllerC WCW,
pubmed-author:MesquitaS FSF,
pubmed-author:MortonC CCC,
pubmed-author:PereiraAA,
pubmed-author:PierpontM EME,
pubmed-author:QuadrelliRR,
pubmed-author:RomeoGG,
pubmed-author:SeidmanC ECE,
pubmed-author:SeidmanJ GJG,
pubmed-author:SilengoMM,
pubmed-author:VaglioAA,
pubmed-author:WeremowiczSS
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pubmed:issnType |
Print
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pubmed:day |
16
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pubmed:volume |
96
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2919-24
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:10077612-Adult,
pubmed-meshheading:10077612-Amino Acid Sequence,
pubmed-meshheading:10077612-Heart Defects, Congenital,
pubmed-meshheading:10077612-Humans,
pubmed-meshheading:10077612-Infant,
pubmed-meshheading:10077612-Limb Deformities, Congenital,
pubmed-meshheading:10077612-Molecular Sequence Data,
pubmed-meshheading:10077612-Mutation,
pubmed-meshheading:10077612-Sequence Analysis, DNA,
pubmed-meshheading:10077612-Syndrome,
pubmed-meshheading:10077612-T-Box Domain Proteins,
pubmed-meshheading:10077612-Transcription Factors
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pubmed:year |
1999
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pubmed:articleTitle |
Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations.
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pubmed:affiliation |
Cardiology Division, Department of Medicine and Department of Cell Biology and Anatomy, Weill Medical College of Cornell University, The New York Hospital, New York, NY 10021, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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