Literature DB >> 16793418

Analysis of gross-chromosomal rearrangements in Saccharomyces cerevisiae.

Kristina H Schmidt1, Vincent Pennaneach, Christopher D Putnam, Richard D Kolodner.   

Abstract

Cells utilize numerous DNA metabolic pathways and cell-cycle checkpoints to maintain the integrity of their genome. Failure of these mechanisms can lead to genome instability, abnormal cell proliferation, and cell death. This chapter describes a method for the measurement of the rate of accumulating gross-chromosomal rearrangements (GCRs) in haploid cells of the yeast Saccharomyces cerevisiae. The isolation of cells with GCRs relies on the simultaneous loss of two counterselectable markers, CAN1 and URA3, within a nonessential region on the left arm of chromosome V. Healing of DNA breaks by de novo telomere addition, translocations, large interstitial deletions, and chromosome fusion has been detected using a PCR-based procedure for the mapping and amplification of breakpoint junctions, which is also described in detail here. This GCR analysis provides an effective tool for the assessment of the contribution by multiple cellular mechanisms to the maintenance of genome integrity.

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Year:  2006        PMID: 16793418     DOI: 10.1016/S0076-6879(05)09027-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  40 in total

1.  Suppression of spontaneous genome rearrangements in yeast DNA helicase mutants.

Authors:  Kristina H Schmidt; Richard D Kolodner
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-17       Impact factor: 11.205

2.  Fluctuation analysis CalculatOR: a web tool for the determination of mutation rate using Luria-Delbruck fluctuation analysis.

Authors:  Brandon M Hall; Chang-Xing Ma; Ping Liang; Keshav K Singh
Journal:  Bioinformatics       Date:  2009-04-15       Impact factor: 6.937

3.  Mechanisms that regulate localization of a DNA double-strand break to the nuclear periphery.

Authors:  Pranav Oza; Sue L Jaspersen; Adriana Miele; Job Dekker; Craig L Peterson
Journal:  Genes Dev       Date:  2009-04-15       Impact factor: 11.361

4.  Double-strand breaks associated with repetitive DNA can reshape the genome.

Authors:  Juan Lucas Argueso; James Westmoreland; Piotr A Mieczkowski; Malgorzata Gawel; Thomas D Petes; Michael A Resnick
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-13       Impact factor: 11.205

5.  The S-phase checkpoint is required to respond to R-loops accumulated in THO mutants.

Authors:  Belén Gómez-González; Irene Felipe-Abrio; Andrés Aguilera
Journal:  Mol Cell Biol       Date:  2009-08-03       Impact factor: 4.272

6.  Determination of gross chromosomal rearrangement rates.

Authors:  Christopher D Putnam; Richard D Kolodner
Journal:  Cold Spring Harb Protoc       Date:  2010-09-01

7.  Defects in DNA lesion bypass lead to spontaneous chromosomal rearrangements and increased cell death.

Authors:  Kristina H Schmidt; Emilie B Viebranz; Lorena B Harris; Hamed Mirzaei-Souderjani; Salahuddin Syed; Robin Medicus
Journal:  Eukaryot Cell       Date:  2009-12-11

8.  Human peroxiredoxin PrxI is an orthologue of yeast Tsa1, capable of suppressing genome instability in Saccharomyces cerevisiae.

Authors:  Ismail Iraqui; Gérard Faye; Sandrine Ragu; Amélie Masurel-Heneman; Richard D Kolodner; Meng-Er Huang
Journal:  Cancer Res       Date:  2008-02-15       Impact factor: 12.701

9.  Chromosome aberrations resulting from double-strand DNA breaks at a naturally occurring yeast fragile site composed of inverted ty elements are independent of Mre11p and Sae2p.

Authors:  Anne M Casper; Patricia W Greenwell; Wei Tang; Thomas D Petes
Journal:  Genetics       Date:  2009-07-27       Impact factor: 4.562

10.  Yeast genome analysis identifies chromosomal translocation, gene conversion events and several sites of Ty element insertion.

Authors:  Yoshiyuki Shibata; Ankit Malhotra; Stefan Bekiranov; Anindya Dutta
Journal:  Nucleic Acids Res       Date:  2009-08-26       Impact factor: 16.971

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