Role of mitochondrial DNA variants in the development of fragile X-associated tremor/ataxia syndrome
Copyright © 2020. Published by Elsevier B.V..
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder that appears in at least one-third of adult carriers of FMR1 premutation. Several studies have shown that mitochondrial dysfunction may play a role in neurodegenerative disorders. In order to assess whether mitochondrial DNA variants are involved in the risk of developing FXTAS we evaluated the frequency of mitochondrial haplogroups in 132 unrelated Spanish FMR1 premutation carriers. In addition, the entire mitogenome of 26 FMR1 premutation carriers was sequenced using massively parallel sequencing technologies to analyze mitochondrial DNA variants. Statistical analyses reveal a significant difference in the frequency of T haplogroup. Data analysis of mitochondrial DNA sequences evidence an association between FXTAS and the burden of heteroplasmic variants as well as their distribution. Our results suggest that haplogroup T might be a potential protective factor for FXTAS and that FXTAS individuals accumulate higher rates of heteroplasmic variants in compromised regions of the mitochondrial genome. These results may explain, in part, the role of mitochondrial DNA in the development of FXTAS.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:52 |
---|---|
Enthalten in: |
Mitochondrion - 52(2020) vom: 15. Mai, Seite 157-162 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Alvarez-Mora, Maria Isabel [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 07.06.2021 Date Revised 07.06.2021 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.mito.2020.03.004 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM30761526X |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM30761526X | ||
003 | DE-627 | ||
005 | 20231225125942.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.mito.2020.03.004 |2 doi | |
028 | 5 | 2 | |a pubmed24n1025.xml |
035 | |a (DE-627)NLM30761526X | ||
035 | |a (NLM)32173566 | ||
035 | |a (PII)S1567-7249(19)30185-0 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Alvarez-Mora, Maria Isabel |e verfasserin |4 aut | |
245 | 1 | 0 | |a Role of mitochondrial DNA variants in the development of fragile X-associated tremor/ataxia syndrome |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 07.06.2021 | ||
500 | |a Date Revised 07.06.2021 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2020. Published by Elsevier B.V. | ||
520 | |a Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder that appears in at least one-third of adult carriers of FMR1 premutation. Several studies have shown that mitochondrial dysfunction may play a role in neurodegenerative disorders. In order to assess whether mitochondrial DNA variants are involved in the risk of developing FXTAS we evaluated the frequency of mitochondrial haplogroups in 132 unrelated Spanish FMR1 premutation carriers. In addition, the entire mitogenome of 26 FMR1 premutation carriers was sequenced using massively parallel sequencing technologies to analyze mitochondrial DNA variants. Statistical analyses reveal a significant difference in the frequency of T haplogroup. Data analysis of mitochondrial DNA sequences evidence an association between FXTAS and the burden of heteroplasmic variants as well as their distribution. Our results suggest that haplogroup T might be a potential protective factor for FXTAS and that FXTAS individuals accumulate higher rates of heteroplasmic variants in compromised regions of the mitochondrial genome. These results may explain, in part, the role of mitochondrial DNA in the development of FXTAS | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a FMR1 premutation | |
650 | 4 | |a FXTAS | |
650 | 4 | |a Low-level heteroplasmic variants | |
650 | 4 | |a Mitogenome | |
650 | 4 | |a Risk factors | |
650 | 4 | |a mtDNA haplogroups | |
650 | 7 | |a DNA, Mitochondrial |2 NLM | |
650 | 7 | |a FMR1 protein, human |2 NLM | |
650 | 7 | |a Fragile X Mental Retardation Protein |2 NLM | |
650 | 7 | |a 139135-51-6 |2 NLM | |
700 | 1 | |a Santos, Cristina |e verfasserin |4 aut | |
700 | 1 | |a Carreño-Gago, Lidia |e verfasserin |4 aut | |
700 | 1 | |a Madrigal, Irene |e verfasserin |4 aut | |
700 | 1 | |a Tejada, Maria Isabel |e verfasserin |4 aut | |
700 | 1 | |a Martinez, Francisco |e verfasserin |4 aut | |
700 | 1 | |a Izquierdo-Alvarez, Silvia |e verfasserin |4 aut | |
700 | 1 | |a Garcia-Arumi, Elena |e verfasserin |4 aut | |
700 | 1 | |a Mila, Montserrat |e verfasserin |4 aut | |
700 | 1 | |a Rodriguez-Revenga, Laia |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Mitochondrion |d 2001 |g 52(2020) vom: 15. Mai, Seite 157-162 |w (DE-627)NLM156856727 |x 1872-8278 |7 nnns |
773 | 1 | 8 | |g volume:52 |g year:2020 |g day:15 |g month:05 |g pages:157-162 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.mito.2020.03.004 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 52 |j 2020 |b 15 |c 05 |h 157-162 |