The Role of Mitochondrial DNA ORIB Polymorphism in Metabolic Syndrome

Pleiades Publishing Ltd - Tập 12 - Trang 59-65 - 2018
D. A. Skuratovskaia1, J. K. Sofronova1, P. A. Zatolokin2, M. A. Vasilenko1, L. S. Litvinova1, I. O. Mazunin1
1Immanuel Kant Baltic Federal University, Kaliningrad, Russia
2Regional Clinical Hospital of the Kaliningrad Region, Kaliningrad, Russia

Tóm tắt

The development of the metabolic syndrome (MS) involves many genes. Certain evidence exists in the literature on the association of polymorphism in the mitochondrial DNA (mtDNA) oriB site, also known as the polycytosine pathway, with the development of insulin resistance, type 2 diabetes mellitus (T2DM) and other metabolic disorders in various ethnic populations. It is suggested that certain polymorphisms at this site are associated with mtDNA copy number in the cell. In this study, using capillary sequencing, we have identified various allelic variants of the mtDNA oriB site in patients with MS (n = 106) and conditionally healthy donors (n = 71). The mtDNA copy number in blood leukocytes was determined by the droplet digital polymerase chain reaction (ddPCR). It has been shown that the variant of the continuous polycytosine tract is significantly more frequent in MS patients with T2DM (p < 0.01). In general, the mtDNA copy number of blood leukocytes was lower in MS patients than in controls. We did not find any correlations between the oriB site variability and the mtDNA copy number.

Tài liệu tham khảo

Sorriento, D., Pascale, A.V., Finelli, R., Carillo, A.L., Annunziata, R., Trimarco, B., and Iaccarino, G., Scientific World Journal, 2014, ID 604685. http://dx.doi.org/.doi 10.1155/2014/604685 Du, C., Fang, M., Li, Y., Li, L., and Wang, X., Cell, 2000, vol. 102, no. 1, pp. 33–42. http://dx.doi.org/. doi 10.1016/S0092-8674(00)00008-8 Marchetti, P., Castedo, M., Susin, S.A., Zamzami, N., Hirsch, T., Macho, A., Haeffner, A., Hirsch, F., Geuskens, M., and Kroemer, G., J. Exp. Med., 1996, vol. 184, no. 3, pp. 1155–1160. doi 10.1084/jem.184.3.1155 Ye, Z., Gillson, C., Sims, M., Khaw, K.T., Plotka, M., Poulton, J., Langenberg, C., and Wareham, N.J., Diabetologia, 2013, vol. 56, no., 9, pp. 1907–1913. doi 10.1007/s00125-013-2945-6 Park, K.S., Chan, J.C., Chuang, L.M., Suzuki, S., Araki, E., Nanjo, K., Ji, L., Ng, M., Nishi, M., Furuta, H., Shirotani, T., Ahn, B.Y., Chung, S.S., Min, H.K., Lee, S.W., Kim, J.H., Cho, Y.M., and Lee, H.K., Diabetologia, 2000, vol. 51, no. 4, pp. 602–608. doi 10.1007/s00125-008-0933-z Poulton, J., Luan, J., Macaulay, V., Hennings, S., Mitchell, J., and Wareham, N.J., Hum. Mol. Genet., 2002, vol. 11, no. 13, pp. 1581–1583. http://dx.doi. org/. doi 10.1016/S0092-8674(00)00099-6 Liou, C.W., Lin, T.K., Huei Weng, H., Lee, C.F., Chen, T.L., Wei, Y.H., Chen, S.D., Chuang, Y.C., Weng, S.W., and Wang, P.W., J. Clin. Endocrinol. Metab., 2007, vol. 92, no. 1, pp. 235–239. doi 10.1210/jc.2006-0653 Chinnery, P.F., Elliott, H.R., Patel, S., Lambert, C., Keers, S.M., Durham, S.E., McCarthy, M.I., Hitman, G.A., Hattersley, A.T., and Walker, M., Lancet, 2005, vol. 366, no. 9497, pp. 1650–1651. doi 10.1016/S0140-6736(05)67492-2 Mohlke, K.L., Jackson, A.U., Scott, L.J., Peck, E.C., Suh, Y.D., Chines, P.S., Watanabe, R.M., Buchanan, T.A., Conneely, K.N., Erdos, M.R., Narisu, N., Enloe, S., Valle, T.T., Tuomilehto, J., Bergman, R.N., Boehnke, M., and Collins, F.S., Hum. Genet., 2005, vol. 118, no. 2, pp. 245–254. doi 10.1007/s00439-005-0046-4 Kim, J.H., Park, K.S., Cho, Y.M., Kang, B.S., Kim, S.K., Jeon, H.J., Kim, S.Y., and Lee, H.K., Diabet Med., 2002, vol. 19, no. 8, pp. 681–684. doi 10.1046/j.1464-5491.2002.00747.x Mueller, E.E., Eder, W., Ebner, S., Schwaiger, E., Santic, D., Kreindl, T., Stanger, O., Paulweber, B., Iglseder, B., Oberkofler, H., Maier, R., Mayr, J.A., Krempler, F., Weitgasser, R., Patsch, W., Sperl, W., and Kofler, B., PLoS One, 2011, vol. 6, no. 1, e16455. doi 10.1371/journal.pone.0016455 Liou, C.W., Lin, T.K., Chen, J.B., Tiao, M.M., Weng, S.W., Chen, S.D., Chuang, Y.C., Chuang, J.H., and Wang, P.W., J. Med. Genet., 2010, vol. 47, no. 11, pp. 723–728. doi 10.1136/jmg.2010.077552 Kwak, S.H. and Park K.S., Front. Biosci. (Landmark Ed.), 2016, vol. 21, pp. 1151–1167. doi 10.2741/4447 Palmieri, V.O., De Rasmo, D., Signorile, A., Sardanelli, A.M., Grattagliano, I., Minerva, F., Cardinale, G., Portincasa, P., Papa, S., and Palasciano, G., Nutrition, 2011, vol. 27, nos. 7–8, pp. 773–777. doi 10.1016/j.nut.2010.08.016 Huang, C.H., Su, S.L., Hsieh, M.C., Cheng, W.L., Chang, C.C., Wu, H.L., Kuo, C.L., Lin, T.T., and Liu, C.S., J. Atheroscler. Thromb., 2011, vol. 18, no. 10, pp. 867–873. doi 10.5551/jat.8698 Peinado, J.R., Diaz-Ruiz, A., Fruhbeck, G., and Malagon, M.M., Proteomics, 2014, vol. 14, nos. 4-5, pp. 452–466. doi 10.1002/pmic.201300376 Xu, F.X., Zhou, X., Shen, F., Pang, R., and Liu, S.M., Diabet Med., 2012, vol. 29, no. 7, e47–54. doi 10.1111/j.1464-5491.2011.03565.x Lee, J.Y., Lee, D.C., Im, J.A., and Lee, J.W., Int. J. Endocrinol., 2014, ID 586017. http://dx.doi.org/. doi 10.1155/2014/586017