Literature DB >> 29043616

Analyzing Genome Rearrangements in Saccharomyces cerevisiae.

Anjana Srivatsan1, Christopher D Putnam1,2, Richard D Kolodner3,4,5,6.   

Abstract

Genome rearrangements underlie different human diseases including many cancers. Determining the rates at which genome rearrangements arise and isolating unique, independent genome rearrangements is critical to understanding the genes and pathways that prevent or promote genome rearrangements. Here, we describe quantitative S. cerevisiae genetic assays for measuring the rates of accumulating genome rearrangements including deletions, translocations, and broken chromosomes healed by de novo telomere addition that result in the deletion of two counter-selectable genes, CAN1 and URA3, placed in the nonessential regions of the S. cerevisiae genome. The assays also allow for the isolation of individual genome rearrangements for structural studies, and a method for analyzing genome rearrangements by next-generation DNA sequencing is provided.

Entities:  

Keywords:  De novo telomere addition; Deletion; Dicentric translocation; GCR rates; Genetics; Genome instability; Monocentric translocation; Whole-genome sequencing

Mesh:

Year:  2018        PMID: 29043616      PMCID: PMC5657460          DOI: 10.1007/978-1-4939-7306-4_5

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  22 in total

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5.  Chromosomal translocations in yeast induced by low levels of DNA polymerase a model for chromosome fragile sites.

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Journal:  Cell       Date:  2005-03-11       Impact factor: 41.582

6.  Mre11-Sae2 and RPA Collaborate to Prevent Palindromic Gene Amplification.

Authors:  Sarah K Deng; Yi Yin; Thomas D Petes; Lorraine S Symington
Journal:  Mol Cell       Date:  2015-11-05       Impact factor: 17.970

7.  A genetic and structural study of genome rearrangements mediated by high copy repeat Ty1 elements.

Authors:  Jason E Chan; Richard D Kolodner
Journal:  PLoS Genet       Date:  2011-05-26       Impact factor: 5.917

8.  Rapid analysis of Saccharomyces cerevisiae genome rearrangements by multiplex ligation-dependent probe amplification.

Authors:  Jason E Chan; Richard D Kolodner
Journal:  PLoS Genet       Date:  2012-03-01       Impact factor: 5.917

9.  Genome-wide screen reveals replication pathway for quasi-palindrome fragility dependent on homologous recombination.

Authors:  Yu Zhang; Natalie Saini; Ziwei Sheng; Kirill S Lobachev
Journal:  PLoS Genet       Date:  2013-12-05       Impact factor: 5.917

10.  A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers.

Authors:  Christopher D Putnam; Anjana Srivatsan; Rahul V Nene; Sandra L Martinez; Sarah P Clotfelter; Sara N Bell; Steven B Somach; Jorge E S de Souza; André F Fonseca; Sandro J de Souza; Richard D Kolodner
Journal:  Nat Commun       Date:  2016-04-13       Impact factor: 14.919

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Journal:  Microb Cell       Date:  2019-01-07

2.  The Saccharomyces cerevisiae Hrq1 and Pif1 DNA helicases synergistically modulate telomerase activity in vitro.

Authors:  David G Nickens; Cody M Rogers; Matthew L Bochman
Journal:  J Biol Chem       Date:  2018-08-01       Impact factor: 5.157

3.  The Swr1 chromatin-remodeling complex prevents genome instability induced by replication fork progression defects.

Authors:  Anjana Srivatsan; Bin-Zhong Li; Barnabas Szakal; Dana Branzei; Christopher D Putnam; Richard D Kolodner
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4.  Mechanisms underlying genome instability mediated by formation of foldback inversions in Saccharomyces cerevisiae.

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Journal:  Elife       Date:  2020-08-07       Impact factor: 8.140

  4 in total

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