Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
35368288
PubMed Central
PMC8968137
DOI
10.3389/fnins.2022.817713
Knihovny.cz E-zdroje
- Klíčová slova
- SLC18A2 gene, neurodegenerative disorders, parkinsonism, trio analysis, whole-exome sequencing,
- Publikační typ
- časopisecké články MeSH
Parkinsonism belongs to the most common neurodegenerative disease. Genetic predisposition could be one of the significant risk factor for disease development. It has been described higher prevalence of parkinsonism in large pedigree from southeastern Moravia region. The study aims were to select accessible subfamily trios from the pedigree suitable for segregation genetic analyses to perform whole exome sequencing (WES) in trio individuals and further to evaluate genetic variants in the each trio. We used IonTorrent platform for WES for five subfamily trios (1-5). Each trio included two affected and one healthy person (as control). Found variants were filtered with respect to MAF < 1% (minor allele frequency), variants effect (based on prediction tools) and disease filter (Parkinsonism responsible genes). Finally, the variants from each trio were assessed with respect to the presence in the patients. There were found no one founder mutation in the subfamilies from the pedigree. Trio 1 shares two variants with trio 2:MC1R:c.322G > A (p.A108T) and MTCL1:c.1445C > T (p.A482V), trio 3 shares two variants with trio 5: DNAJC6:c.1817A > C (p.H606P) and HIVEP3:c.3856C > A (p.R1286W). In trios 4 and 5, there were found two variants in gene CSMD1:c.3335A > G (p.E1112G) and c.4071C > G (p.I1357M) respectively. As the most potentially damaging, we evaluated the non-shared variant SLC18A2:c.583G > A (p.G195S). The variant could affect dopamine transport in dopaminergic neurons. The study of the parkinsonism genetic background in isolated Moravian population suggested that there could be significant accumulation of many risk genetic factors. For verification of the variants influence, it would be appropriate to perform a more extensive population study and suitable functional analysis.
Department of Medical Genetics University Hospital Olomouc Olomouc Czechia
Department of Neurology Faculty of Medicine and Dentistry Palacký University Olomouc Olomouc Czechia
Department of Neurology University Hospital Olomouc Olomouc Czechia
Zobrazit více v PubMed
Allen C. E., Mak C. H., Wu L. C. (2002). The kappa B transcriptional enhancer motif and signal sequences of V(D)J recombination are targets for the zinc finger protein HIVEP3/KRC: a site selection amplification binding study. PubMed DOI PMC
Ando M., Fiesel F. C., Hudec R., Caulfield T. R., Ogaki K., Górka-Skoczylas P., et al. (2017). The PINK1 p.I368N mutation affects protein stability and ubiquitin kinase activity. PubMed DOI PMC
Bandres-Ciga S., Diez-Fairen M., Kim J. J., Singleton A. B. (2020). Genetics of Parkinson’s disease: an introspection of its journey towards precision medicine. PubMed DOI PMC
Brighina L., Riva C., Bertola F., Saracchi E., Fermi S., Goldwurm S., et al. (2013). Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson’s disease. PubMed DOI PMC
Buervenich S., Carmine A., Galter D., Shahabi H. N., Johnels B., Holmberg B., et al. (2005). A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample. PubMed DOI
Campêlo C. L. C., Cagni F. C., de Siqueira Figueredo D., Oliveira L. G., Jr., Silva-Neto A. B., Macêdo P. T., et al. (2017). Variants in SNCA gene are associated with parkinson’s disease risk and cognitive symptoms in a brazilian sample. PubMed DOI PMC
Chartier-Harlin M. C., Dachsel J. C., Vilariño-Güell C., Lincoln S. J., Leprêtre F., Hulihan M. M., et al. (2011). Translation initiator EIF4G1 mutations in familial Parkinson disease. PubMed DOI PMC
Dolgacheva L. P., Berezhnov A. V., Fedotova E. I., Zinchenko V. P., Abramov A. Y. (2019). Role of DJ-1 in the mechanism of pathogenesis of Parkinson’s disease. PubMed DOI PMC
Edvardson S., Cinnamon Y., Ta-Shma A., Shaag A., Yim Y. I., Zenvirt S., et al. (2012). A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism. PubMed DOI PMC
Farlow J. L., Robak L. A., Hetrick K., Bowling K., Boerwinkle E., Coban-Akdemir Z. H., et al. (2016). Whole-Exome sequencing in familial parkinson disease. PubMed DOI PMC
Gan-Or Z., Mohsin N., Girard S. L., Montplaisir J. Y., Ambalavanan A., Strong S., et al. (2016). The role of the melanoma gene MC1R in Parkinson disease and REM sleep Behavior Disorder. PubMed DOI PMC
Gao X., Simon K. C., Han J., Schwarzschild M. A., Ascherio A. (2009). Genetic determinants of hair color and Parkinson’s disease risk. PubMed DOI PMC
Gazal S., Gosset S., Verdura E., Bergametti F., Guey S., Babron M. C., et al. (2016). Can whole-exome sequencing data be used for linkage analysis? PubMed DOI PMC
Guo J. F., Zhang L., Li K., Mei J. P., Xue J., Chen J., et al. (2018). Coding mutations in NUS1 contribute to Parkinson’s disease. PubMed DOI PMC
Håvik B., Le Hellard S., Rietschel M., Lybæk H., Djurovic S., Mattheisen M., et al. (2011). The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia. PubMed DOI
Hughes A. J., Daniel S. E., Ben-Shlomo Y., Lees A. J. (2002). The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. PubMed DOI
Kalinderi K., Bostantjopoulou S., Fidani L. (2016). The genetic background of Parkinson’s disease: current progress and future prospects. PubMed DOI
Köroğlu Ç, Baysal L., Cetinkaya M., Karasoy H., Tolun A. (2013). DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability. PubMed DOI
Kraus D. M., Elliott G. S., Chute H., Horan T., Pfenninger K. H., Sanford S. D., et al. (2006). CSMD1 is a novel multiple domain complement-regulatory protein highly expressed in the central nervous system and epithelial tissues. PubMed DOI
Lin G., Lee P. T., Chen K., Mao D., Tan K. L., Zuo Z., et al. (2018). Phospholipase PLA2G6, a parkinsonism-associated gene, affects Vps26 and Vps35, retromer function, and ceramide levels, similar to α-Synuclein gain. PubMed DOI
Liu Y., Edwards R. H. (1997). The role of vesicular transport proteins in synaptic transmission and neural degeneration. PubMed DOI
Lopez O. L., Smith G., Meltzer C. C., Becker J. T. (1999). Dopamine systems in human immunodeficiency virus-associated dementia. PubMed
Marti T., Puig-Butille J. A., Potrony M., Badenas C., Milà M., Malvehy J., et al. (2015). The MC1R melanoma risk variant p.R160W is associated with Parkinson disease. PubMed DOI
Mensikova K., Kanovsky P., Kaiserova M., Mikulicova L., Vastik M., Hlustik P., et al. (2013). Prevalence of neurodegenerative parkinsonism in an isolated population in south-eastern moravia, czech republic. PubMed DOI
Mensikova K., Kaňovský P., Otruba P., Kaiserová M., Vastik M., Hlustik P., et al. (2014). Epidemiological study of neurodegenerative Parkinsonism in “Hornacko”, a specific region of the south-eastern moravia, czech republic. DOI
Miller S. A., Dykes D. D., Polesky H. F. (1988). A simple salting out procedure for extracting DNA from human nucleated cells. PubMed DOI PMC
Mir R., Tonelli F., Lis P., Macartney T., Polinski N. K., Martinez T. N., et al. (2018). The Parkinson’s disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human. PubMed DOI PMC
Mosharov E. V., Larsen K. E., Kanter E., Phillips K. A., Wilson K., Schmitz Y., et al. (2009). Interplay between cytosolic dopamine, calcium, and alpha-synuclein causes selective death of substantia nigra neurons. PubMed DOI PMC
Ortega R. A., Wang C., Raymond D., Bryant N., Scherzer C. R., Thaler A., et al. (2021). Association of dual LRRK2 G2019S and GBA variations with parkinson disease progression. PubMed DOI PMC
Park J. S., Blair N. F., Sue C. M. (2015). The role of ATP13A2 in Parkinson’s disease: clinical phenotypes and molecular mechanisms. PubMed DOI
Ruiz-Martínez J., Azcona L. J., Bergareche A., Martí-Massó J. F., Paisán-Ruiz C. (2017). Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease. PubMed DOI PMC
Sato Y., Akitsu M., Amano Y., Yamashita K., Ide M., Shimada K., et al. (2013). The novel PAR-1-binding protein MTCL1 has crucial roles in organizing microtubules in polarizing epithelial cells. PubMed DOI
Schwalbe M., Biernat J., Bibow S., Ozenne V., Jensen M. R., Kadavath H., et al. (2013). Phosphorylation of human Tau protein by microtubule affinity-regulating kinase 2. PubMed DOI
Thiriot D. S., Sievert M. K., Ruoho A. E. (2002). Identification of human vesicle monoamine transporter (VMAT2) lumenal cysteines that form an intramolecular disulfide bond. PubMed DOI
Toma C., Díaz-Gay M., Franch-Expósito S., Arnau-Collell C., Overs B., Muñoz J., et al. (2020). Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer. PubMed DOI PMC
Vodicka R., Kolarikova K., Vrtel R., Mensikova K., Kanovsky P., Prochazka M. (2020). “Evaluating basic next-generation sequencing parameters in relation to true/false positivity findings of rare variants in an isolated population from the Czech Republic South-Eastern Moravia Region with a high incidence of parkinsonism,” in DOI
Xiromerisiou G., Bourinaris T., Houlden H., Lewis P. A., Senkevich K., Hammer M., et al. (2021). SORL1 mutation in a Greek family with Parkinson’s disease, and dementia. PubMed DOI PMC
Yemni E. A., Monies D., Alkhairallah T., Bohlega S., Abouelhoda M., Magrashi A., et al. (2019). Integrated analysis of whole exome sequencing and copy number evaluation in Parkinson’s Disease. PubMed DOI PMC
Yi W., MacDougall E. J., Tang M. Y., Krahn A. I., Gan-Or Z., Trempe J. F., et al. (2019). The landscape of Parkin variants reveals pathogenic mechanisms and therapeutic targets in Parkinson’s disease. PubMed DOI PMC
Yim Y. I., Sun T., Wu L. G., Raimondi A., De Camilli P., Eisenberg E., et al. (2010). Endocytosis and clathrin-uncoating defects at synapses of auxilin knockout mice. PubMed DOI PMC
Endemic parkinsonism: clusters, biology and clinical features