2021  1,540
2020  1,374
2019  1,023
2018  0,932
2017  0,977
2016  0,799
2015  0,662
2014  0,740
2013  0,739
2012  0,637
2011  0,658
2010  0,654
2009  0,570
2008  0,849
2007  0,805
2006  0,330
2005  0,435
2004  0,623
2003  0,567
2002  0,641
2001  0,490
2000  0,477
1999  0,762
1998  0,785
1997  0,507
1996  0,518
1995  0,502
Vol 48(2014) N 5 p. 655-663; DOI 10.1134/S0026893314050136 Full Text

I.O. Suchkova1*, L.I. Pavlinova 1,2, E.E. Larionova 1, N.V. Alenina4, K.V. Solovyov1, T.V. Baranova1, E.V. Belotcerkovskay1, L.K. Sasina1, M. Bader4, A.D. Denisenko1, O.E. Mustafina3, E.K. Khusnutdinova3, E.L. Patkin1

Length Polymorphism of the B2-VNTR Minisatellite Repeat of the Bradykinin B2 Receptor Gene in Healthy Russians and Patients with Coronary Heart Disease

1Institute of Experimental Medicine, Northwest Branch, Russian Academy of Medical Sciences, St. Petersburg, 197376 Russia
2Pavlov Institute of Physiology, Russian Academy of Sciences, St. Petersburg, 199034 Russia
3Institute of Biochemistry and Genetics, Ufa Research Center, Russian Academy of Sciences, Ufa, 450054 Russia
4Max-Delbrück-Center for Molecular Medicine, Berlin-Buch, 13125 Germany

Received - 2014-03-16; Accepted - 2014-04-07

Bradykinin B2 receptor is involved in many processes, including the regulation of blood pressure and smooth muscle contraction, vasodilation, inflammation, edema, cell proliferation, and pain. This receptor attracts special attention as one of the factors that have cardioprotective and infarct-limiting effects. Certain genetic variants of the coding and noncoding regions of the bradykinin B2 receptor gene (BDKRB2) may play a role in modulating its expression. The 3-untranslated region of BDKRB2 exon 3 harbors a minisatellite repeat (B2-VNTR), which affects the mRNA stability. Hence, it is of interest to study a possible association of B2-VNRT alleles with various forms of coronary heart disease (CHD). In our work the allele and genotype frequency distributions of B2-VNTR were compared between healthy individuals and patients with CHD (angina pectoris or myocardial infarction (MI)) of the Russian ethnic group. Based on its length polymorphism, B2-VNTR was classed with low-polymorphic non-hypervariable minisatellites. Three B2-VNTR alleles, which consisted of 43, 38, and 33 repeats, were observed in all investigated cohorts. The alleles with 43 and 33 repeats were the most prevalent. The allele and genotype frequencies of B2-VNTR did not significantly differ between males and females in control group, and also between healthy males and males with angina pectoris or MI. Thus, B2-VNTR length polymorphism was not associated with these clinical forms of CHD in males. However, we do not exclude the possibility of an association of the short B2-VNTR alleles (38 and 33repeats) with a cardio protective effect in females with CHD. This hypothesis requires further investigation.

minisatellite repeats, B2-VNTR, allele polymorphism, bradykinin B2 receptor, PCR, coronary heart disease, angina pectoris, myocardial infarction