Literature DB >> 15545718

Molecular evolution of the human chromosome 15 pericentromeric region.

D P Locke1, Z Jiang, L M Pertz, D Misceo, N Archidiacono, E E Eichler.   

Abstract

We present a detailed molecular evolutionary analysis of 1.2 Mb from the pericentromeric region of human 15q11. Sequence analysis indicates the region has been subject to extensive interchromosomal and intrachromosomal duplications during primate evolution. Comparative FISH analyses among non-human primates show remarkable quantitative and qualitative differences in the organization and duplication history of this region - including lineage-specific deletions and duplication expansions. Phylogenetic and comparative analyses reveal that the region is composed of at least 24 distinct segmental duplications or duplicons that have populated the pericentromeric regions of the human genome over the last 40 million years of human evolution. The value of combining both cytogenetic and experimental data in understanding the complex forces which have shaped these regions is discussed. Copyright (c) 2005 S. Karger AG, Basel.

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Mesh:

Year:  2005        PMID: 15545718     DOI: 10.1159/000080804

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  15 in total

1.  Genetic structure of the Spanish population.

Authors:  Javier Gayán; José J Galan; Antonio González-Pérez; María Eugenia Sáez; María Teresa Martínez-Larrad; Carina Zabena; M Carmen Rivero; Ana Salinas; Reposo Ramírez-Lorca; Francisco J Morón; Jose Luis Royo; Concha Moreno-Rey; Juan Velasco; José M Carrasco; Eva Molero; Carolina Ochoa; María Dolores Ochoa; Marta Gutiérrez; Mercedes Reina; Rocío Pascual; Alejandro Romo-Astorga; Juan Luis Susillo-González; Enrique Vázquez; Luis M Real; Agustín Ruiz; Manuel Serrano-Ríos
Journal:  BMC Genomics       Date:  2010-05-25       Impact factor: 3.969

2.  Retrotransposon accumulation and satellite amplification mediated by segmental duplication facilitate centromere expansion in rice.

Authors:  Jianxin Ma; Scott A Jackson
Journal:  Genome Res       Date:  2005-12-14       Impact factor: 9.043

3.  The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function.

Authors:  Tanguy Araud; Sharon Graw; Ralph Berger; Michael Lee; Estele Neveu; Daniel Bertrand; Sherry Leonard
Journal:  Biochem Pharmacol       Date:  2011-06-28       Impact factor: 5.858

4.  A human-specific, truncated α7 nicotinic receptor subunit assembles with full-length α7 and forms functional receptors with different stoichiometries.

Authors:  Matías Lasala; Jeremías Corradi; Ariana Bruzzone; María Del Carmen Esandi; Cecilia Bouzat
Journal:  J Biol Chem       Date:  2018-05-21       Impact factor: 5.157

5.  A genome-wide survey of structural variation between human and chimpanzee.

Authors:  Tera L Newman; Eray Tuzun; V Anne Morrison; Karen E Hayden; Mario Ventura; Sean D McGrath; Mariano Rocchi; Evan E Eichler
Journal:  Genome Res       Date:  2005-09-16       Impact factor: 9.043

Review 6.  The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function.

Authors:  Melissa L Sinkus; Sharon Graw; Robert Freedman; Randal G Ross; Henry A Lester; Sherry Leonard
Journal:  Neuropharmacology       Date:  2015-02-19       Impact factor: 5.250

7.  Evolutionary dynamics of segmental duplications from human Y-chromosomal euchromatin/heterochromatin transition regions.

Authors:  Stefan Kirsch; Claudia Münch; Zhaoshi Jiang; Ze Cheng; Lin Chen; Christiane Batz; Evan E Eichler; Werner Schempp
Journal:  Genome Res       Date:  2008-04-29       Impact factor: 9.043

8.  Punctuated duplication seeding events during the evolution of human chromosome 2p11.

Authors:  Julie E Horvath; Cassandra L Gulden; Rhea U Vallente; Marla Y Eichler; Mario Ventura; John D McPherson; Tina A Graves; Richard K Wilson; Stuart Schwartz; Mariano Rocchi; Evan E Eichler
Journal:  Genome Res       Date:  2005-06-17       Impact factor: 9.043

9.  Effect of CHRFAM7A Δ2bp gene variant on secondary inflammation after spinal cord injury.

Authors:  Mingkuan Lin; Wan Huang; Nadine Kabbani; Mark M Theiss; John F Hamilton; James M Ecklund; Yvette P Conley; Yoram Vodovotz; David Brienza; Amy K Wagner; Emily Robbins; Gwendolyn A Sowa; Robert H Lipsky
Journal:  PLoS One       Date:  2021-05-06       Impact factor: 3.240

10.  Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.

Authors:  Yong-Hui Jiang; Kekio Wauki; Qian Liu; Jan Bressler; Yanzhen Pan; Catherine D Kashork; Lisa G Shaffer; Arthur L Beaudet
Journal:  BMC Genomics       Date:  2008-01-28       Impact factor: 3.969

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