Literature DB >> 26294667

Preferential Breakpoints in the Recovery of Broken Dicentric Chromosomes in Drosophila melanogaster.

Hunter Hill1, Kent G Golic2.   

Abstract

We designed a system to determine whether dicentric chromosomes in Drosophila melanogaster break at random or at preferred sites. Sister chromatid exchange in a Ring-X chromosome produced dicentric chromosomes with two bridging arms connecting segregating centromeres as cells divide. This double bridge can break in mitosis. A genetic screen recovered chromosomes that were linearized by breakage in the male germline. Because the screen required viability of males with this X chromosome, the breakpoints in each arm of the double bridge must be closely matched to produce a nearly euploid chromosome. We expected that most linear chromosomes would be broken in heterochromatin because there are no vital genes in heterochromatin, and breakpoint distribution would be relatively unconstrained. Surprisingly, approximately half the breakpoints are found in euchromatin, and the breakpoints are clustered in just a few regions of the chromosome that closely match regions identified as intercalary heterochromatin. The results support the Laird hypothesis that intercalary heterochromatin can explain fragile sites in mitotic chromosomes, including fragile X. Opened rings also were recovered after male larvae were exposed to X-rays. This method was much less efficient and produced chromosomes with a strikingly different array of breakpoints, with almost all located in heterochromatin. A series of circularly permuted linear X chromosomes was generated that may be useful for investigating aspects of chromosome behavior, such as crossover distribution and interference in meiosis, or questions of nuclear organization and function.
Copyright © 2015 by the Genetics Society of America.

Entities:  

Keywords:  FLP; dicentric chromosome; fragile X; intercalary heterochromatin

Mesh:

Substances:

Year:  2015        PMID: 26294667      PMCID: PMC4596669          DOI: 10.1534/genetics.115.181156

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  36 in total

1.  Broken chromosomal ends can be elongated by conversion in Drosophila melanogaster.

Authors:  S Mikhailovsky; T Belenkaya; P Georgiev
Journal:  Chromosoma       Date:  1999-05       Impact factor: 4.316

2.  A new resource for characterizing X-linked genes in Drosophila melanogaster: systematic coverage and subdivision of the X chromosome with nested, Y-linked duplications.

Authors:  R Kimberley Cook; Megan E Deal; Jennifer A Deal; Russell D Garton; C Adam Brown; Megan E Ward; Rachel S Andrade; Eric P Spana; Thomas C Kaufman; Kevin R Cook
Journal:  Genetics       Date:  2010-09-27       Impact factor: 4.562

3.  Chromosome ends in Drosophila without telomeric DNA sequences.

Authors:  H Biessmann; S B Carter; J M Mason
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

4.  HipHop interacts with HOAP and HP1 to protect Drosophila telomeres in a sequence-independent manner.

Authors:  Guanjun Gao; Jean-Claude Walser; Michelle L Beaucher; Patrizia Morciano; Natalia Wesolowska; Jie Chen; Yikang S Rong
Journal:  EMBO J       Date:  2010-01-07       Impact factor: 11.598

5.  Telomere loss provokes multiple pathways to apoptosis and produces genomic instability in Drosophila melanogaster.

Authors:  Simon W A Titen; Kent G Golic
Journal:  Genetics       Date:  2008-10-09       Impact factor: 4.562

6.  The FLP recombinase of yeast catalyzes site-specific recombination in the Drosophila genome.

Authors:  K G Golic; S Lindquist
Journal:  Cell       Date:  1989-11-03       Impact factor: 41.582

7.  Control of DNA replication and spatial distribution of defined DNA sequences in salivary gland cells of Drosophila melanogaster.

Authors:  M P Hammond; C D Laird
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

8.  Association of fragile X syndrome with delayed replication of the FMR1 gene.

Authors:  R S Hansen; T K Canfield; M M Lamb; S M Gartler; C D Laird
Journal:  Cell       Date:  1993-07-02       Impact factor: 41.582

9.  Nonrandom distribution of interhomolog recombination events induced by breakage of a dicentric chromosome in Saccharomyces cerevisiae.

Authors:  Wei Song; Malgorzata Gawel; Margaret Dominska; Patricia W Greenwell; Einat Hazkani-Covo; Kerry Bloom; Thomas D Petes
Journal:  Genetics       Date:  2013-02-14       Impact factor: 4.562

10.  Preferential transposition of Drosophila P elements to nearby chromosomal sites.

Authors:  J Tower; G H Karpen; N Craig; A C Spradling
Journal:  Genetics       Date:  1993-02       Impact factor: 4.562

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  2 in total

1.  Homolog-Dependent Repair Following Dicentric Chromosome Breakage in Drosophila melanogaster.

Authors:  Jayaram Bhandari; Travis Karg; Kent G Golic
Journal:  Genetics       Date:  2019-05-03       Impact factor: 4.562

2.  The processivity factor Pol32 mediates nuclear localization of DNA polymerase delta and prevents chromosomal fragile site formation in Drosophila development.

Authors:  Jingyun Ji; Xiaona Tang; Wen Hu; Keith A Maggert; Yikang S Rong
Journal:  PLoS Genet       Date:  2019-05-17       Impact factor: 5.917

  2 in total

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