Literature DB >> 9215666

Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity.

E E Eichler1, M L Budarf, M Rocchi, L L Deaven, N A Doggett, A Baldini, D L Nelson, H W Mohrenweiser.   

Abstract

A 9.7 kb segment encompassing exons 7-10 of the adrenoleukodystrophy (ALD) locus of the X chromosome has duplicated to specific locations near the pericentromeric regions of human chromosomes 2p11,10p11, 16p11 and 22q11. Comparative sequence analysis reveals 92-96% nucleotide identity, indicating that the autosomal ALD paralogs arose relatively recently during the course of higher primate evolution (5-10 million years ago). Analysis of sequences flanking the duplication region identifies the presence of an unusual GCTTTTTGC repeat which may be a sequence-specific integration site for the process of pericentromeric-directed transposition. The breakpoint sequence and phylogenetic analysis predict a two-step transposition model, in which a duplication from Xq28 to pericentromeric 2p11 occurred once, followed by a rapid distribution of a larger duplicon cassette among the pericentromeric regions. In addition to facilitating more effective mutation detection among ALD patients, these findings provide further insight into the molecular basis underlying a pericentromeric-directed mechanism for non-homologous interchromosomal exchange.

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Year:  1997        PMID: 9215666     DOI: 10.1093/hmg/6.7.991

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  41 in total

1.  Localization of mariner DNA transposons in the human genome by PRINS.

Authors:  L T Reiter; T Liehr; B Rautenstrauss; H M Robertson; J R Lupski
Journal:  Genome Res       Date:  1999-09       Impact factor: 9.043

2.  The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome.

Authors:  J E Horvath; S Schwartz; E E Eichler
Journal:  Genome Res       Date:  2000-06       Impact factor: 9.043

3.  A contiguous 3-Mb sequence-ready map in the S3-MX region on 21q22.2 based on high- throughput nonisotopic library screenings.

Authors:  T Hildmann; X Kong; J O'Brien; L Riesselman; H M Christensen; E Dagand; H Lehrach; M L Yaspo
Journal:  Genome Res       Date:  1999-04       Impact factor: 9.043

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

Authors:  Michel van Geel; Evan E Eichler; Amy F Beck; Zhihong Shan; Thomas Haaf; Silvère M van der Maarel; Rune R Frants; Pieter J de Jong
Journal:  Am J Hum Genet       Date:  2001-11-30       Impact factor: 11.025

5.  Segmental duplications: organization and impact within the current human genome project assembly.

Authors:  J A Bailey; A M Yavor; H F Massa; B J Trask; E E Eichler
Journal:  Genome Res       Date:  2001-06       Impact factor: 9.043

6.  Efficient approach to unique single-nucleotide polymorphism discovery.

Authors:  P Taillon-Miller; E E Piernot; P Y Kwok
Journal:  Genome Res       Date:  1999-05       Impact factor: 9.043

Review 7.  X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.

Authors:  K D Smith; S Kemp; L T Braiterman; J F Lu; H M Wei; M Geraghty; G Stetten; J S Bergin; J Pevsner; P A Watkins
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

8.  Pericentromeric duplications in the laboratory mouse.

Authors:  James W Thomas; Mary G Schueler; Tyrone J Summers; Robert W Blakesley; Jennifer C McDowell; Pamela J Thomas; Jacquelyn R Idol; Valerie V B Maduro; Shih-Queen Lee-Lin; Jeffrey W Touchman; Gerard G Bouffard; Stephen M Beckstrom-Sternberg; Eric D Green
Journal:  Genome Res       Date:  2003-01       Impact factor: 9.043

9.  Genome architecture catalyzes nonrecurrent chromosomal rearrangements.

Authors:  Paweł Stankiewicz; Christine J Shaw; Jason D Dapper; Keiko Wakui; Lisa G Shaffer; Marjorie Withers; Leah Elizondo; Sung-Sup Park; James R Lupski
Journal:  Am J Hum Genet       Date:  2003-03-20       Impact factor: 11.025

Review 10.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

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