Using gene-network landscape to dissect genotype effects of TCF7L2 genetic variant on diabetes and cardiovascular risk


Autoria(s): Vaquero, Andre R.; Ferreira, Noely E.; Omae, Samantha V.; Rodrigues, Mariliza V.; Teixeira, Samantha K.; Krieger, Jose E.; Pereira, Alexandre C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Vaquero AR, Ferreira NE, Omae SV, Rodrigues MV, Teixeira SK, Krieger JE, Pereira AC. Using gene-network landscape to dissect genotype effects of TCF7L2 genetic variant on diabetes and cardiovascular risk. Physiol Genomics 44: 903-914, 2012. First published August 7, 2012; doi:10.1152/physiolgenomics.00030.2012.-The single nucleotide polymorphism (SNP) within the TCF7L2 gene, rs7903146, is, to date, the most significant genetic marker associated with Type 2 diabetes mellitus (T2DM) risk. Nonetheless, its functional role in disease pathology is poorly understood. The aim of the present study was to investigate, in vascular smooth muscle cells from 92 patients undergoing aortocoronary bypass surgery, the contribution of this SNP in T2DM using expression levels and expression correlation comparison approaches, which were visually represented as gene interaction networks. Initially, the expression levels of 41 genes (seven TCF7L2 splice forms and 40 other T2DM relevant genes) were compared between rs7903146 wild-type (CC) and T2DM-risk (CT + TT) genotype groups. Next, we compared the expression correlation patterns of these 41 genes between groups to observe if the relationships between genes were different. Five TCF7L2 splice forms and nine genes showed significant expression differences between groups. RXR alpha gene was pinpointed as showing the most different expression correlation pattern with other genes. Therefore, T2DM risk alleles appear to be influencing TCF7L2 splice form's expression in vascular smooth muscle cells, and RXR alpha gene is pointed out as a treatment target candidate for risk reduction in individuals with high risk of developing T2DM, especially individuals harboring TCF7L2 risk genotypes.

National Council for Scientific and Technological Development (CNPq)

National Council for Scientific and Technological Development (CNPq)

Sao Paulo Research Foundation (FAPESP)

Sao Paulo Research Foundation (FAPESP)

Identificador

PHYSIOLOGICAL GENOMICS, BETHESDA, v. 44, n. 19, supl. 1, Part 1, pp. 903-914, OCT, 2012

1094-8341

http://www.producao.usp.br/handle/BDPI/41390

10.1152/physiolgenomics.00030.2012

http://dx.doi.org/10.1152/physiolgenomics.00030.2012

Idioma(s)

eng

Publicador

AMER PHYSIOLOGICAL SOC

BETHESDA

Relação

PHYSIOLOGICAL GENOMICS

Direitos

restrictedAccess

Copyright AMER PHYSIOLOGICAL SOC

Palavras-Chave #CORRELATION NETWORKS #DIFFERENTIAL EXPRESSION #DIFFERENTIAL COEXPRESSION #TYPE 2 DIABETES MELLITUS #GENOME-WIDE ASSOCIATION #SMOOTH-MUSCLE-CELLS #HUMAN PANCREATIC-ISLETS #X-RECEPTOR-ALPHA #SUSCEPTIBILITY LOCI #PPAR-GAMMA #COMMON VARIANTS #TYPE-2 #EXPRESSION #RETINOIDS #CELL BIOLOGY #GENETICS & HEREDITY #PHYSIOLOGY
Tipo

article

original article

publishedVersion