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 AbstractInfluence of enzymatic extrusion liquefaction pretreatment for Chinese rice wine on the volatiles generated from extruded rice    Next AbstractEffects of a catalytic volatile particle remover (VPR) on the particulate matter emissions from a direct injection spark ignition engine »

Genetics


Title:"Identification of SAS4 and SAS5, two genes that regulate silencing in Saccharomyces cerevisiae"
Author(s):Xu EY; Kim S; Replogle K; Rine J; Rivier DH;
Address:"Department of Cell and Structural Biology, University of Illinois, Urbana, Illinois 61801, USA"
Journal Title:Genetics
Year:1999
Volume:153
Issue:1
Page Number:13 - 23
DOI: 10.1093/genetics/153.1.13
ISSN/ISBN:0016-6731 (Print) 0016-6731 (Linking)
Abstract:"In Saccharomyces cerevisiae, chromatin-mediated silencing inactivates transcription of the genes at the HML and HMR cryptic mating-type loci and genes near telomeres. Mutations in the Rap1p and Abf1p binding sites of the HMR-E silencer (HMRa-e**) result in a loss of silencing at HMR. We characterized a collection of 15 mutations that restore the alpha-mating phenotype to MATalpha HMRa-e** strains. These mutations defined three complementation groups, two new groups and one group that corresponded to the previously identified SAS2 gene. We cloned the genes that complemented members of the new groups and identified two previously uncharacterized genes, which we named SAS4 and SAS5. Neither SAS4 nor SAS5 was required for viability. Null alleles of SAS4 and SAS5 restored SIR4-dependent silencing at HMR, establishing that each is a regulator of silencing. Null alleles of SAS4 and SAS5 bypassed the role of the Abf1p binding site of the HMR-E silencer but not the role of the ACS or Rap1p binding site. Previous analysis indicated that SAS2 is homologous to a human gene that is a site of recurring translocations involved in acute myeloid leukemia. Similarly, SAS5 is a member of a gene family that included two human genes that are the sites of recurring translocations involved in acute myeloid leukemia"
Keywords:"Amino Acid Sequence Binding Sites DNA-Binding Proteins/metabolism Fungal Proteins/chemistry/*genetics/metabolism/physiology *Gene Expression Regulation, Fungal/drug effects Genes, Fungal/genetics/physiology Genes, Mating Type, Fungal Genetic Complementati;"
Notes:"MedlineXu, E Y Kim, S Replogle, K Rine, J Rivier, D H eng 5T32-GM07283/GM/NIGMS NIH HHS/ GM-31105/GM/NIGMS NIH HHS/ GM-52103/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1999/09/03 Genetics. 1999 Sep; 153(1):13-23. doi: 10.1093/genetics/153.1.13"

 
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 16-11-2024