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Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago.

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TLDR
The evolutionary history of chromosome 6 in primates was investigated in detail and it was found that the primate ancestor had a homologous chromosome with the same marker order, but with the centromere located at 6p22.1.
Abstract
Molecular cytogenetics provides a visual, pictorial record of the tree of life, and in this respect the fusion origin of human chromosome 2 is a well-known paradigmatic example. Here we report on a variant chromosome 6 in which the centromere jumped to 6p22.1. ChIP-chip experiments with antibodies against the centromeric proteins CENP-A and CENPC exactly defined the neocentromere as lying at chr6:26,407–26,491 kb. We investigated in detail the evolutionary history of chromosome 6 in primates and found that the primate ancestor had a homologous chromosome with the same marker order, but with the centromere located at 6p22.1. Sometime between 17 and 23 million years ago (Mya), in the common ancestor of humans and apes, the centromere of chromosome 6 moved from 6p22.1 to its current location. The neocentromere we discovered, consequently, has jumped back to the ancestral position, where a latent centromereforming potentiality persisted for at least 17 Myr. Because all living organisms form a tree of life, as first conceived by Darwin, evolutionary perspectives can provide compelling underlying explicative grounds for contemporary genomic phenomena.

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The common marmoset genome provides insight into primate biology and evolution

Kim C. Worley, +120 more
- 01 Jan 2014 - 
TL;DR: The whole-genome sequence of the common marmoset enables increased power for comparative analyses among available primate genomes and facilitates biomedical research application.
Journal ArticleDOI

Centromere repositioning in mammals

TL;DR: A review of the centromere repositioning is provided, new data on the population genetics of the ENC of the orangutan is added, and for the first time an ENC is described on the X chromosome of squirrel monkeys.
Journal ArticleDOI

Complete genomic and epigenetic maps of human centromeres

- 01 Apr 2022 - 
TL;DR: In this paper , a complete, telomere-to-telomere human genome assembly (T2T-CHM13) has enabled the comprehensively characterize pericentromeric and centromeric repeats, which constitute 6.2% of the genome.
Journal ArticleDOI

Neocentromeres and epigenetically inherited features of centromeres.

TL;DR: Analysis of neocentromeres found in human clinical samples and induced in model organisms distinguishes features of centromeres that are dependent on centromere DNA from features that are epigenetically inherited together with the formation of a functional kinetochore.
Journal ArticleDOI

Centromere inactivation and epigenetic modifications of a plant chromosome with three functional centromeres

TL;DR: A transmissible chromosome with multiple centromeres in wheat that encompassed one large and two small domains containing the centromeric histone CENH3 showed characteristics typical to dicentric chromosomes, including chromosome breaks and centromere inactivation.
References
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Journal ArticleDOI

Initial sequencing and analysis of the human genome.

Eric S. Lander, +248 more
- 15 Feb 2001 - 
TL;DR: The results of an international collaboration to produce and make freely available a draft sequence of the human genome are reported and an initial analysis is presented, describing some of the insights that can be gleaned from the sequence.
Journal ArticleDOI

The origin of man: a chromosomal pictorial legacy

TL;DR: A comparative analysis of high-resolution chromosomes from orangutan, gorilla, chimpanzee, and man suggests that 18 or 23 pairs of chromosomes of modern man are virtually identical to those of the authors' "common hominoid ancestor", with the remaining pairs slightly different.
Journal ArticleDOI

Catarrhine primate divergence dates estimated from complete mitochondrial genomes: concordance with fossil and nuclear DNA evidence.

TL;DR: The entire mitochondrial DNA genomes from a representative of three cercopithecoid tribes are sequenced, and divergence dates using a penalized likelihood and a Bayesian method are estimated, both of which take into account the effects of rate differences on lineages, phylogenetic tree structure, and multiple calibration points.
Journal ArticleDOI

Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution

TL;DR: The genome rearrangement analysis of the human and mouse genomes implies the existence of a large number of very short “hidden” synteny blocks that were invisible in the comparative mapping data and ignored in the random breakage model, suggesting a model of chromosome evolution that postulates that mammalian genomes are mosaics of fragile regions with high propensity for rearrangements and solid regions with low propensity for reorganisation.
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