Source:http://linkedlifedata.com/resource/pubmed/id/15969004
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
2005-6-22
|
pubmed:abstractText |
To investigate the function of ALK3 gene, the gene regulation and the signaling pathway related to ventricular septum defect during heart development. The model mice with ALK3 gene knock-out via alpha-MHC-Cre/lox P system were bred. The mRNA expression level of control group was compared with that of experiment group and ALK3 downstream genes were screened using PCR-select cDNA subtraction microarray. The mRNA of control group was extracted from E11.5 normal mouse hearts, and that of experiment group, from E11.5 hearts of mice with alpha-MHC Cre(+/-) ALK3(F/+) genotype. It was found that the mice with ALK3 gene knock-out produced heart defects involving the interventricular septum. The platelet-activating factors acetylhydrolase and the transcription factor Pax-8 and so on, were down-regulated. However, the Protein Tyrosine Kinase (PTK) of Focal Adhesion Kinase (FAK) subfamily and beta subtype protein 14-3-3 were up-regulated in the alpha-MHC Cre(+/-) ALK3(F/-) mice. These data provide support that ALK3 gene played an important role during heart development. The platelet-activating factors acetylhydrolase and Pax-8 genes could be important ALK3 downstream genes in the BMP signaling pathway during interventricular septum development. PTK and beta subtype protein 14-3-3 might be regulatory factors in this pathway.
|
pubmed:language |
chi
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1-Alkyl-2-acetylglycerophosphocholin...,
http://linkedlifedata.com/resource/pubmed/chemical/14-3-3 Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Bmpr1a protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Bone Morphogenetic Protein...,
http://linkedlifedata.com/resource/pubmed/chemical/Paired Box Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Pax8 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
1000-3061
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
19
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
267-71
|
pubmed:meshHeading |
pubmed-meshheading:15969004-1-Alkyl-2-acetylglycerophosphocholine Esterase,
pubmed-meshheading:15969004-14-3-3 Proteins,
pubmed-meshheading:15969004-Animals,
pubmed-meshheading:15969004-Bone Morphogenetic Protein Receptors, Type I,
pubmed-meshheading:15969004-Genotype,
pubmed-meshheading:15969004-Heart Septal Defects, Ventricular,
pubmed-meshheading:15969004-Mice,
pubmed-meshheading:15969004-Mice, Knockout,
pubmed-meshheading:15969004-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:15969004-Paired Box Transcription Factors,
pubmed-meshheading:15969004-Protein-Tyrosine Kinases,
pubmed-meshheading:15969004-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:15969004-Signal Transduction
|
pubmed:year |
2003
|
pubmed:articleTitle |
[Preliminary study of ALK3 downstream genes related to ventricular septum defect].
|
pubmed:affiliation |
Department of Cardiology, The First Affiliated Hospital of Wenzhou Medical College, Wenzhou 325000, China. Deyeyang@hotmail.com
|
pubmed:publicationType |
Journal Article,
English Abstract
|