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Haplogroup JT

From Wikipedia, the free encyclopedia
(Redirected fromHaplogroup JT (mtDNA))
Human mitochondrial DNA
Haplogroup JT
Possible time of origin50,300 YBP
Possible place of originWest Asia
AncestorR2'JT
DescendantsJ,T
Defining mutations11251, 15452A, 16126[1]

Haplogroup JT is ahuman mitochondrial DNA (mtDNA) haplogroup.

Origin

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Haplogroup JT is descended from the macro-haplogroupR. It is the ancestral clade to the mitochondrial haplogroupsJ andT.

Distribution

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JT (predominantlyJ) was found among the ancientEtruscans.[2] The root level haplogroup JT* has been assigned to an ancient person found at the Colfiorito necropolis inUmbria in central Italy.[3]

The haplogroup has also been found amongIberomaurusian specimens dating from theEpipaleolithic at theTaforalt prehistoric site.[4] One ancient individual carried a haplotype, which correlates with either the JT clade or the haplogroupH subclade H14b1 (1/9; 11%).[5]

Subclades

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Tree

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This phylogenetic tree of haplogroup JT subclades is based on the paper by Mannis van Oven and Manfred KayserUpdated comprehensive phylogenetic tree of global human mitochondrial DNA variation[1] and subsequent published research.

Health

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Maternally inherited ancient mtDNA variants have clear impact on the presentation of disease in a modern society. Superhaplogroup JT is an example of reduced risk of Parkinson's disease[6] And mitochondrial and mtDNa alterations continue to be promising disease biomarkers.[7][8]

See also

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Phylogenetic tree ofhuman mitochondrial DNA (mtDNA) haplogroups

 Mitochondrial Eve (L)  
L0L1–6 
L1L2 L3  L4L5L6
MN 
CZDEGQ OASR IWXY
CZBFR0 pre-JT P U
HVJTK
HVJT

References

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  1. ^abvan Oven, Mannis; Manfred Kayser (13 Oct 2008)."Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation".Human Mutation.30 (2):E386 –E394.doi:10.1002/humu.20921.PMID 18853457.
  2. ^"We Are Not Our Ancestors". Archived fromthe original on 2009-04-08. Retrieved2012-02-10.
  3. ^GenBank Accession number: MN687309.1
  4. ^Bernard Secher; Rosa Fregel; José M Larruga; Vicente M Cabrera; Phillip Endicott; José J Pestano; Ana M González (2014)."The history of the North African mitochondrial DNA haplogroup U6 gene flow into the African, Eurasian and American continents".BMC Evolutionary Biology.14 (1): 109.Bibcode:2014BMCEE..14..109S.doi:10.1186/1471-2148-14-109.PMC 4062890.PMID 24885141.
  5. ^Kefi, Rym; et al. (2016). "On the origin of Iberomaurusians: new data based on ancient mitochondrial DNA and phylogenetic analysis of Afalou and Taforalt populations".Mitochondrial DNA Part A.29 (1):147–157.doi:10.1080/24701394.2016.1258406.PMID 28034339.S2CID 4490910.
  6. ^Marom S, Friger M, Mishmar D (February 2017)."MtDNA meta-analysis reveals both phenotype specificity and allele heterogeneity: a model for differential association".Sci Rep.7 43449.doi:10.1038/srep43449.PMC 5322532.PMID 28230165.
  7. ^Martín-Jiménez R, Lurette O, Hebert-Chatelain E (August 2020). "Damage in Mitochondrial DNA Associated with Parkinson's Disease".DNA Cell Biol.39 (8):1421–1430.doi:10.1089/dna.2020.5398.PMID 32397749.
  8. ^Lowes H, Pyle A, Duddy M, Hudson G (May 2019)."Cell-free mitochondrial DNA in progressive multiple sclerosis".Mitochondrion.46:307–312.doi:10.1016/j.mito.2018.07.008.PMC 6509276.PMID 30098422.

External links

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