Human rs6265 (196G>A) polymorphism in the BDNF gene is associated with many clinically significant phenotypic manifestations. Rhesus monkey (Macaca mulatta) has a functionally significant rs309950446 ( 136G>A) polymorphism. To determine this polymorphism in macaques, we used mismatch amplification mutation assay (MAMA)-PCR method with non-complementary nucleotide to the template chain at the 3rd position from the 3’-end of the allele-specific primers (mismatch primers), which allowed the best discrimination of the alleles. Genotyping of male rhesus monkeys (n=178) and cynomolgus monkeys (Macaca fascicularis) (n=90) was carried out. The A/A, G/G, and G/A genotypes were found in 16, 34, and 50% rhesus macaques, respectively. In the cynomolgus macaques, the mutant polymorphic allele was not detected. The study results allow considering rhesus macaques as a potential biological model for assessment of the gen—environment interaction of the BDNF gene polymorphism.
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References
Huang EJ, Reichardt LF. Neurotrophins: roles in neuronal development and function. Ann. Rev. Neurosci. 2001;24:677-736. doi: https://doi.org/10.1146/annurev.neuro.24.1.677
Pencea V, Bingaman KD, Wiegand SJ, Luskin MB. Infusion of brain-derived neurotrophic factor into the lateral ventricle of the adult rat leads to new neurons in the parenchyma of the striatum, septum, thalamus, and hypothalamus. J. Neurosci. 2001;21(17):6706-6717. doi: https://doi.org/10.1523/JNEUROSCI.21-17-06706.2001
Iu ECY, Chan CB. Is Brain-Derived Neurotrophic Factor a metabolic hormone in peripheral tissues? Biology (Basel). 2022;11(7):1063. doi: https://doi.org/10.3390/biology11071063
Baj G, Carlino D, Gardossi L, Tongiorgi E. Toward a unified biological hypothesis for the BDNF Val66Met-associated memory deficits in humans: a model of impaired dendritic mRNA trafficking. Front. Neurosci. 2013;7:188. doi: https://doi.org/10.3389/fnins.2013.00188
Bekinschtein P, Cammarota M, Katche C, Slipczuk L, Rossato JI, Goldin A, Izquierdo I, Medina JH. BDNF is essential to promote persistence of long-term memory storage. Proc. Natl Acad. Sci. USA. 2008;105(7):2711-2716. doi: https://doi.org/10.1073/pnas.0711863105
Youssef MM, Underwood MD, Huang YY, Hsiung SC, Liu Y, Simpson NR, Bakalian MJ, Rosoklija GB, Dwork AJ, Arango V, Mann JJ. Association of BDNF Val66Met polymorphism and brain BDNF Levels with major depression and suicide. Int. J. Neuropsychopharmacol. 2018;21(6):528-538. doi: https://doi.org/10.1093/ijnp/pyy008
Borroni B, Archetti S, Costanzi C, Grassi M, Ferrari M, Radeghieri A, Caimi L, Caltagirone C, Di Luca M, Padovani A; ITINAD Working Group. Role of BDNF Val66Met functional polymorphism in Alzheimer’s disease-related depression. Neurobiol. Aging. 2009;30(9):1406-1412. doi: https://doi.org/10.1016/j.neurobiolaging.2007.11.023
Dincheva I, Lynch NB, Lee FS. The role of BDNF in the development of fear learning. Depress Anxiety. 2016;33(10):907-916. doi: https://doi.org/10.1002/da.22497
Sanchez MM, Das D, Taylor JL, Noda A, Yesavage JA, Salehi A. BDNF polymorphism predicts the rate of decline in skilled task performance and hippocampal volume in healthy individuals. Transl. Psychiatry. 2011;1(10):e51. doi: https://doi.org/10.1038/tp.2011.47.
Lu B, Nagappan G, Guan X, Nathan PJ, Wren P. BDNFbased synaptic repair as a disease-modifying strategy for neurodegenerative diseases. Nat. Rev. Neurosci. 2013;14(6):401-416. doi: https://doi.org/10.1038/nrn3505
Verhagen M, van der Meij A, van Deurzen PA, Janzing JG, Arias-Vásquez A, Buitelaar JK, Franke B. Meta-analysis of the BDNF Val66Met polymorphism in major depressive disorder: effects of gender and ethnicity. Mol. Psychiatry. 2010;15(3):260-271. doi: https://doi.org/10.1038/mp.2008.109
Cirulli F, Reif A, Herterich S, Lesch KP, Berry A, Francia N, Aloe L, Barr CS, Suomi SJ, Alleva E. A novel BDNF polymorphism affects plasma protein levels in interaction with early adversity in rhesus macaques. Psychoneuroendocrinology. 2011;36(3):372-379. doi: https://doi.org/10.1016/j.psyneuen.2010.10.019
Pavlova LE, Panchenko AlV, Timina MF, Gvozdik TE, Kovalenko VV, Agumava AA, Panchenko AV. Genetic homogeneity of the population of male rhesus macaques by the polymorphisms of genes oprm1, npy, maoa, crh, 5-htt as determined by cluster analysis of blood count data. Russ. J. Genet. 2022;58(4):420-427. doi: https://doi.org/10.1134/S1022795422030097
Deekshit VK, Jazeela K, Chakraborty G, Rohit A, Chakraborty A, Karunasaga I. Mismatch amplification mutation assay-polymerase chain reaction: A method of detecting fluoroquinolone resistance mechanism in bacterial pathogens. Indian J. Med. Res. 2019;149(2):146-150. doi: https://doi.org/10.4103/ijmr.IJMR_2091_17
Terracciano A, Piras MG, Lobina M, Mulas A, Meirelles O, Sutin AR, Chan W, Sanna S, Uda M, Crisponi L, Schlessinger D. Genetics of serum BDNF: meta-analysis of the Val66Met and genome-wide association study. World J. Biol. Psychiatry. 2013;14(8):583-589. doi: https://doi.org/10.3109/15622975.2011.616533
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Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 175, No. 3, pp. 374-378, March, 2023
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Pavlova, L.E., Timina, M.F., Agumava, A.A. et al. Genotyping of Macaque Population on the Brain-Derived Neurotrophic Factor Gene Polymorphism by Mismatch Amplification Mutation Assay (MAMA)-PCR. Bull Exp Biol Med 175, 388–392 (2023). https://doi.org/10.1007/s10517-023-05873-4
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DOI: https://doi.org/10.1007/s10517-023-05873-4