Literature DB >> 18997000

Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.

Hidehito Inagaki1, Tamae Ohye, Hiroshi Kogo, Takema Kato, Hasbaira Bolor, Mariko Taniguchi, Tamim H Shaikh, Beverly S Emanuel, Hiroki Kurahashi.   

Abstract

Chromosomal aberrations have been thought to be random events. However, recent findings introduce a new paradigm in which certain DNA segments have the potential to adopt unusual conformations that lead to genomic instability and nonrandom chromosomal rearrangement. One of the best-studied examples is the palindromic AT-rich repeat (PATRR), which induces recurrent constitutional translocations in humans. Here, we established a plasmid-based model that promotes frequent intermolecular rearrangements between two PATRRs in HEK293 cells. In this model system, the proportion of PATRR plasmid that extrudes a cruciform structure correlates to the levels of rearrangement. Our data suggest that PATRR-mediated translocations are attributable to unusual DNA conformations that confer a common pathway for chromosomal rearrangements in humans.

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Year:  2008        PMID: 18997000      PMCID: PMC2652202          DOI: 10.1101/gr.079244.108

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  42 in total

1.  Pkd1 unusual DNA conformations are recognized by nucleotide excision repair.

Authors:  A Bacolla; A Jaworski; T D Connors; R D Wells
Journal:  J Biol Chem       Date:  2001-02-27       Impact factor: 5.157

2.  Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).

Authors:  H Kurahashi; T H Shaikh; P Hu; B A Roe; B S Emanuel; M L Budarf
Journal:  Hum Mol Genet       Date:  2000-07-01       Impact factor: 6.150

3.  Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males.

Authors:  H Kurahashi; B S Emanuel
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

4.  Trinucleotide expansion in haploid germ cells by gap repair.

Authors:  I V Kovtun; C T McMurray
Journal:  Nat Genet       Date:  2001-04       Impact factor: 38.330

5.  Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm.

Authors:  Takema Kato; Kouji Yamada; Hidehito Inagaki; Hiroshi Kogo; Tamae Ohye; Beverly S Emanuel; Hiroki Kurahashi
Journal:  Fertil Steril       Date:  2007-04-19       Impact factor: 7.329

6.  The Mre11 complex is required for repair of hairpin-capped double-strand breaks and prevention of chromosome rearrangements.

Authors:  Kirill S Lobachev; Dmitry A Gordenin; Michael A Resnick
Journal:  Cell       Date:  2002-01-25       Impact factor: 41.582

7.  The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.

Authors:  Hiroki Kurahashi; Tamim Shaikh; Masayuki Takata; Tatsushi Toda; Beverly S Emanuel
Journal:  Am J Hum Genet       Date:  2003-01-29       Impact factor: 11.025

Review 8.  Roles of transition nuclear proteins in spermiogenesis.

Authors:  Marvin L Meistrich; Bhagyalaxmi Mohapatra; Cynthia R Shirley; Ming Zhao
Journal:  Chromosoma       Date:  2003-02-06       Impact factor: 4.316

9.  Rapid, stabilizing palindrome rearrangements in somatic cells by the center-break mechanism.

Authors:  Lesley A Cunningham; Atina G Coté; Cennet Cam-Ozdemir; Susanna M Lewis
Journal:  Mol Cell Biol       Date:  2003-12       Impact factor: 4.272

10.  A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).

Authors:  Manjunath A Nimmakayalu; Anthony L Gotter; Tamim H Shaikh; Beverly S Emanuel
Journal:  Hum Mol Genet       Date:  2003-09-02       Impact factor: 6.150

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  47 in total

1.  Searching for non-B DNA-forming motifs using nBMST (non-B DNA motif search tool).

Authors:  R Z Cer; K H Bruce; D E Donohue; N A Temiz; U S Mudunuri; M Yi; N Volfovsky; A Bacolla; B T Luke; J R Collins; R M Stephens
Journal:  Curr Protoc Hum Genet       Date:  2012-04

2.  Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.

Authors:  Maoqing Tong; Takema Kato; Kouji Yamada; Hidehito Inagaki; Hiroshi Kogo; Tamae Ohye; Makiko Tsutsumi; Jieru Wang; Beverly S Emanuel; Hiroki Kurahashi
Journal:  Hum Mol Genet       Date:  2010-04-13       Impact factor: 6.150

3.  Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome.

Authors:  Aaron R Quinlan; Royden A Clark; Svetlana Sokolova; Mitchell L Leibowitz; Yujun Zhang; Matthew E Hurles; Joshua C Mell; Ira M Hall
Journal:  Genome Res       Date:  2010-03-22       Impact factor: 9.043

4.  Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.

Authors:  Stuart A Scott; Ninette Cohen; Tracy Brandt; Peter E Warburton; Lisa Edelmann
Journal:  Hum Mol Genet       Date:  2010-06-22       Impact factor: 6.150

Review 5.  The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.

Authors:  H Kurahashi; H Inagaki; T Ohye; H Kogo; M Tsutsumi; T Kato; M Tong; B S Emanuel
Journal:  Clin Genet       Date:  2010-10       Impact factor: 4.438

6.  Paternal origin of the de novo constitutional t(11;22)(q23;q11).

Authors:  Tamae Ohye; Hidehito Inagaki; Hiroshi Kogo; Makiko Tsutsumi; Takema Kato; Maoqing Tong; Merryn V E Macville; Livija Medne; Elaine H Zackai; Beverly S Emanuel; Hiroki Kurahashi
Journal:  Eur J Hum Genet       Date:  2010-02-24       Impact factor: 4.246

7.  Non-B DNA-forming sequences and WRN deficiency independently increase the frequency of base substitution in human cells.

Authors:  Albino Bacolla; Guliang Wang; Aklank Jain; Nadia A Chuzhanova; Regina Z Cer; Jack R Collins; David N Cooper; Vilhelm A Bohr; Karen M Vasquez
Journal:  J Biol Chem       Date:  2011-02-01       Impact factor: 5.157

8.  G-quadruplex structures formed at the HOX11 breakpoint region contribute to its fragility during t(10;14) translocation in T-cell leukemia.

Authors:  Mridula Nambiar; Mrinal Srivastava; Vidya Gopalakrishnan; Sritha K Sankaran; Sathees C Raghavan
Journal:  Mol Cell Biol       Date:  2013-09-03       Impact factor: 4.272

Review 9.  DNA secondary structures: stability and function of G-quadruplex structures.

Authors:  Matthew L Bochman; Katrin Paeschke; Virginia A Zakian
Journal:  Nat Rev Genet       Date:  2012-10-03       Impact factor: 53.242

Review 10.  The cellular etiology of chromosome translocations.

Authors:  Vassilis Roukos; Bharat Burman; Tom Misteli
Journal:  Curr Opin Cell Biol       Date:  2013-03-14       Impact factor: 8.382

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