Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractPrediction of blood:air and fat:air partition coefficients of volatile organic compounds for the interpretation of data in breath gas analysis    Next AbstractA rapid method for breath analysis in cystic fibrosis patients »

Mol Cell Biol


Title:"Two different types of double-strand breaks in Saccharomyces cerevisiae are repaired by similar RAD52-independent, nonhomologous recombination events"
Author(s):Kramer KM; Brock JA; Bloom K; Moore JK; Haber JE;
Address:"Rosenstiel Basic Medical Sciences Research Center, Brandeis University, Waltham, Massachusetts 02254-9110"
Journal Title:Mol Cell Biol
Year:1994
Volume:14
Issue:2
Page Number:1293 - 1301
DOI: 10.1128/mcb.14.2.1293-1301.1994
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"In haploid rad52 Saccharomyces cerevisiae strains unable to undergo homologous recombination, a chromosomal double-strand break (DSB) can be repaired by imprecise rejoining of the broken chromosome ends. We have used two different strategies to generate broken chromosomes: (i) a site-specific DSB generated at the MAT locus by HO endonuclease cutting or (ii) a random DSB generated by mechanical rupture during mitotic segregation of a conditionally dicentric chromosome. Broken chromosomes were repaired by deletions that were highly variable in size, all of which removed more sequences than was required either to prevent subsequent HO cleavage or to eliminate a functional centromere, respectively. The junction of the deletions frequently occurred where complementary strands from the flanking DNA could anneal to form 1 to 5 bp, although 12% (4 of 34) of the events appear to have occurred by blunt-end ligation. These types of deletions are very similar to the junctions observed in the repair of DSBs by mammalian cells (D. B. Roth and J. H. Wilson, Mol. Cell. Biol. 6:4295-4304, 1986). When a high level of HO endonuclease, expressed in all phases of the cell cycle, was used to create DSBs, we also recovered a large class of very small (2- or 3-bp) insertions in the HO cleavage site. These insertions appear to represent still another mechanism of DSB repair, apparently by annealing and filling in the overhanging 3' ends of the cleavage site. These types of events have also been well documented for vertebrate cells"
Keywords:"Base Sequence Chromosome Mapping Chromosomes, Fungal *DNA Damage DNA Primers DNA, Fungal/genetics/metabolism DNA-Binding Proteins/biosynthesis/*genetics Fungal Proteins/biosynthesis/*genetics *Genes, Fungal Mating Factor Mitosis Molecular Sequence Data Mu;"
Notes:"MedlineKramer, K M Brock, J A Bloom, K Moore, J K Haber, J E eng GM07122/GM/NIGMS NIH HHS/ GM32238/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. 1994/02/01 Mol Cell Biol. 1994 Feb; 14(2):1293-301. doi: 10.1128/mcb.14.2.1293-1301.1994"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024