New apolipoprotein A-V: comparative genomics meets metabolism
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12678656
Knihovny.cz E-zdroje
- MeSH
- apolipoprotein A-V MeSH
- apolipoproteiny A MeSH
- apolipoproteiny genetika metabolismus MeSH
- druhová specificita MeSH
- genetická predispozice k nemoci genetika MeSH
- genomika metody MeSH
- haplotypy MeSH
- hyperlipidemie genetika metabolismus MeSH
- jednonukleotidový polymorfismus genetika MeSH
- krysa rodu Rattus MeSH
- lidé MeSH
- metabolismus lipidů * MeSH
- molekulární sekvence - údaje MeSH
- myši MeSH
- regulace genové exprese genetika MeSH
- sekvence aminokyselin MeSH
- sekvenční homologie MeSH
- sekvenční seřazení MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- APOA5 protein, human MeSH Prohlížeč
- Apoa5 protein, mouse MeSH Prohlížeč
- apolipoprotein A-V MeSH
- apolipoproteiny A MeSH
- apolipoproteiny MeSH
The availability of the human genome sequence and the recently completed draft sequences of two major mammalian model species, the mouse (Mus musculus) and the rat (Rattus norvegicus), allow researchers to apply novel approaches for gene identification and characterization, using methods of comparative and functional genomics. Recently, a new gene coding for apolipoprotein A-V was identified in the vicinity of APOA-I/C-III/A-IV cluster on human chromosome 11q23 by comparative sequencing method. In a relatively short time, compelling evidence accumulated for the substantial role of APOA-V in lipid metabolism. Studies in knock-out and transgenic mice revealed that its expression pattern correlates negatively with triglyceride levels. This observation was verified in human population studies in variety of ethnic and age groups. Several single nucleotide polymorphisms were described and particular SNP alleles and haplotypes in the APO A-V gene region were shown to be associated with dyslipidemia. The discovery and characterization of the APO A-V demonstrates current possibilities of the integrative approaches in biology, boosted by the available bioinformatic tools.
APOAV (T-1131>C) variant has no effect on mother's height in a large population study