Literature DB >> 16763779

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!

Hassan Hassani-Kumleh1, Massoud Houshmand, Mehdi Shafa Shariat Panahi, Gholam Hossein Riazi, Mohammad Hossein Sanati, Kurosh Gharagozli, Mojdeh Ghabaee.   

Abstract

: Multiple Sclerosis (MS) is a multifocal demyelinating central nervous system disorder in which interplay between genes and the environment are supposed to be involved. Mitochondrial DNA (mtDNA) has the only non-coding regions at the displacement loop (D-loop) region that contains two hypervariable segments (HVS-I and HVS-II) with high polymorphism. mtDNA has already been fully sequenced and many subsequent publications have showed polymorphic sites, haplogroups and haplotypes. Haplogroups could have important implications to understand association between mutability of the mitochondrial genome and disease. To assess relationship between mtDNA haplogroups and MS, we have sequenced the mtDNA HVS-I in 54 MS patients and 100 control subjects. We have found that haplogroups A and K are significantly more abundant in MS patients (P=0.042 for haplogroup A and P=0.0005 for haplogroup K). Thus, these two haplogroups might act synergistically to increase the penetrance of MS disease.

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Year:  2006        PMID: 16763779     DOI: 10.1007/s10571-006-9026-z

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  24 in total

Review 1.  Transcription and replication of mitochondrial DNA.

Authors:  D A Clayton
Journal:  Hum Reprod       Date:  2000-07       Impact factor: 6.918

Review 2.  Genetic analysis of multiple sclerosis.

Authors:  Alastair Compston; Stephen Sawcer
Journal:  Curr Neurol Neurosci Rep       Date:  2002-05       Impact factor: 5.081

Review 3.  Genetics of multiple sclerosis: determinants of autoimmunity and neurodegeneration.

Authors:  Bernadette Kalman; Ross H Albert; Thomas P Leist
Journal:  Autoimmunity       Date:  2002-07       Impact factor: 2.815

4.  Evolutionary correlation between control region sequence and restriction polymorphisms in the mitochondrial genome of a large Senegalese Mandenka sample.

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Journal:  Mol Biol Evol       Date:  1995-03       Impact factor: 16.240

5.  mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.

Authors:  A Torroni; M T Lott; M F Cabell; Y S Chen; L Lavergne; D C Wallace
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

6.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

7.  Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?

Authors:  M Arnestad; S H Opdal; M A Musse; A Vege; T O Rognum
Journal:  Acta Paediatr       Date:  2002       Impact factor: 2.299

8.  Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.

Authors:  S Hofmann; R Bezold; M Jaksch; B Obermaier-Kusser; S Mertens; P Kaufhold; W Rabl; W Hecker; K D Gerbitz
Journal:  Genomics       Date:  1997-01-01       Impact factor: 5.736

9.  Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease.

Authors:  T Ozawa; M Tanaka; H Ino; K Ohno; T Sano; Y Wada; M Yoneda; Y Tanno; T Miyatake; T Tanaka
Journal:  Biochem Biophys Res Commun       Date:  1991-04-30       Impact factor: 3.575

10.  Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

Authors:  A Torroni; M Petrozzi; L D'Urbano; D Sellitto; M Zeviani; F Carrara; C Carducci; V Leuzzi; V Carelli; P Barboni; A De Negri; R Scozzari
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

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  5 in total

1.  Stressed cybrids model demyelinated axons in multiple sclerosis.

Authors:  Laura Llobet; Aurora Gómez-Durán; Ruth Iceta; Eldris Iglesias; Julio Montoya; Jesús Martín-Martínez; José Ramón Ara; Eduardo Ruiz-Pesini
Journal:  Metab Brain Dis       Date:  2013-04-24       Impact factor: 3.584

2.  Do haplogroups H and U act to increase the penetrance of Alzheimer's disease?

Authors:  Farzaneh Fesahat; Massoud Houshmand; Mehdi Shafa Shariat Panahi; Kurosh Gharagozli; Farzaneh Mirzajani
Journal:  Cell Mol Neurobiol       Date:  2006-12-21       Impact factor: 4.231

3.  The Role of Mitochondria in AMD: Current Knowledge and Future Applications.

Authors:  Mohammad Riazi-Esfahani; Baruch D Kuppermann; M Cristina Kenney
Journal:  J Ophthalmic Vis Res       Date:  2017 Oct-Dec

4.  Variants of Mitochondrial Genome and Risk of Multiple Sclerosis Development in Russians.

Authors:  M S Kozin; O G Kulakova; I S Kiselev; O P Balanovsky; A N Boyko; O O Favorova
Journal:  Acta Naturae       Date:  2018 Oct-Dec       Impact factor: 1.845

Review 5.  Oldies but Goldies mtDNA Population Variants and Neurodegenerative Diseases.

Authors:  Patrick F Chinnery; Aurora Gomez-Duran
Journal:  Front Neurosci       Date:  2018-10-12       Impact factor: 4.677

  5 in total

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