Literature DB >> 11731935

A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes.

Michel van Geel1, Evan E Eichler, Amy F Beck, Zhihong Shan, Thomas Haaf, Silvère M van der Maarel, Rune R Frants, Pieter J de Jong.   

Abstract

Subtelomeric duplications of an obscure tubulin "genic" segment located near the telomere of human chromosome 4q35 have occurred at different evolutionary time points within the last 25 million years of the catarrhine (i.e., hominoid and Old World monkey) evolution. The analyses of these segments reported here indicate an exceptional level of evolutionary instability. Substantial intra- and interspecific differences in copy number and distribution are observed among cercopithecoid (Old World monkey) and hominoid genomes. Characterization of the hominoid duplicated segments reveals a strong positional bias within pericentromeric and subtelomeric regions of the genome. On the basis of phylogenetic analysis from predicted proteins and comparisons of nucleotide-substitution rates, we present evidence of a conserved b-tubulin gene among the duplications. Remarkably, the evolutionary conservation has occurred in a nonorthologous fashion, such that the functional copy has shifted its positional context between hominoids and cercopithecoids. We propose that, in a chimpanzee-human common ancestor, one of the paralogous copies assumed the original function, whereas the ancestral copy acquired mutations and eventually became silenced. Our analysis emphasizes the dynamic nature of duplication-mediated genome evolution and the delicate balance between gene acquisition and silencing.

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Year:  2001        PMID: 11731935      PMCID: PMC419983          DOI: 10.1086/338307

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  25 in total

1.  The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements.

Authors:  M van Geel; L J Heather; R Lyle; J E Hewitt; R R Frants; P J de Jong
Journal:  Genomics       Date:  1999-10-01       Impact factor: 5.736

2.  Codon-substitution models for heterogeneous selection pressure at amino acid sites.

Authors:  Z Yang; R Nielsen; N Goldman; A M Pedersen
Journal:  Genetics       Date:  2000-05       Impact factor: 4.562

3.  Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35.

Authors:  M van Geel; J C van Deutekom; A van Staalduinen; R J Lemmers; M C Dickson; M H Hofker; G W Padberg; J E Hewitt; P J de Jong; R R Frants
Journal:  Cytogenet Cell Genet       Date:  2000

Review 4.  Distal-less-related homeobox genes of vertebrates: evolution, function, and regulation.

Authors:  T Zerucha; M Ekker
Journal:  Biochem Cell Biol       Date:  2000       Impact factor: 3.626

5.  Large multi-chromosomal duplications encompass many members of the olfactory receptor gene family in the human genome.

Authors:  B J Trask; H Massa; V Brand-Arpon; K Chan; C Friedman; O T Nguyen; E Eichler; G van den Engh; S Rouquier; H Shizuya; D Giorgi
Journal:  Hum Mol Genet       Date:  1998-12       Impact factor: 6.150

Review 6.  Masquerading repeats: paralogous pitfalls of the human genome.

Authors:  E E Eichler
Journal:  Genome Res       Date:  1998-08       Impact factor: 9.043

7.  Base-calling of automated sequencer traces using phred. I. Accuracy assessment.

Authors:  B Ewing; L Hillier; M C Wendl; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

8.  Consed: a graphical tool for sequence finishing.

Authors:  D Gordon; C Abajian; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

9.  FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates.

Authors:  Z Shan; B Zabel; U Trautmann; U Hillig; C Ottolenghi; Y Wan; T Haaf
Journal:  Eur J Hum Genet       Date:  2000-03       Impact factor: 4.246

10.  The Tarsius gamma-globin gene: pseudogene or active gene?

Authors:  C M Meireles; J Czelusniak; M Goodman
Journal:  Mol Phylogenet Evol       Date:  1999-11       Impact factor: 4.286

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  13 in total

1.  Mapping and initial analysis of human subtelomeric sequence assemblies.

Authors:  Harold Riethman; Anthony Ambrosini; Carlos Castaneda; Jeffrey Finklestein; Xue-Lan Hu; Uma Mudunuri; Sheila Paul; Jun Wei
Journal:  Genome Res       Date:  2004-01       Impact factor: 9.043

2.  Serial segmental duplications during primate evolution result in complex human genome architecture.

Authors:  Pawełl Stankiewicz; Christine J Shaw; Marjorie Withers; Ken Inoue; James R Lupski
Journal:  Genome Res       Date:  2004-11       Impact factor: 9.043

3.  FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients.

Authors:  T Rijkers; G Deidda; S van Koningsbruggen; M van Geel; R J L F Lemmers; J C T van Deutekom; D Figlewicz; J E Hewitt; G W Padberg; R R Frants; S M van der Maarel
Journal:  J Med Genet       Date:  2004-11       Impact factor: 6.318

4.  Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16.

Authors:  Violaine Goidts; Justyna M Szamalek; Pieter J de Jong; David N Cooper; Nadia Chuzhanova; Horst Hameister; Hildegard Kehrer-Sawatzki
Journal:  Genome Res       Date:  2005-09       Impact factor: 9.043

5.  Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event.

Authors:  M Katharine Rudd; Raelynn M Endicott; Cynthia Friedman; Megan Walker; Janet M Young; Kazutoyo Osoegawa; Pieter J de Jong; Eric D Green; Barbara J Trask
Journal:  Genome Res       Date:  2008-10-24       Impact factor: 9.043

Review 6.  Human subtelomere structure and variation.

Authors:  H Riethman; A Ambrosini; S Paul
Journal:  Chromosome Res       Date:  2005       Impact factor: 5.239

7.  Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosome.

Authors:  Justyna M Szamalek; Violaine Goidts; Nadia Chuzhanova; Horst Hameister; David N Cooper; Hildegard Kehrer-Sawatzki
Journal:  Hum Genet       Date:  2005-05-10       Impact factor: 4.132

8.  Chromosome r(10)(p15.3q26.12) in a newborn child: case report.

Authors:  Cecilia Gunnarsson; Barbara Graffmann; Jon Jonasson
Journal:  Mol Cytogenet       Date:  2009-12-07       Impact factor: 2.009

9.  Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p.

Authors:  Jane Guy; Tom Hearn; Moira Crosier; Jonathan Mudge; Luigi Viggiano; Dirk Koczan; Hans-Jurgen Thiesen; Jeffrey A Bailey; Julie E Horvath; Evan E Eichler; Mark E Earthrowl; Panos Deloukas; Lisa French; Jane Rogers; David Bentley; Michael S Jackson
Journal:  Genome Res       Date:  2003-02       Impact factor: 9.043

10.  Duplication and relocation of the functional DPY19L2 gene within low copy repeats.

Authors:  Andrew R Carson; Joseph Cheung; Stephen W Scherer
Journal:  BMC Genomics       Date:  2006-03-09       Impact factor: 3.969

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