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 AbstractBreakthrough during air sampling with polyurethane foam: What do PUF 2/PUF 1 ratios mean?    Next Abstract[Effects of allelochemical dibutyl phthalate on Gymnodinium breve reactive oxygen species] »

Funct Integr Genomics


Title:Large-scale identification of genes important for apical growth in Saccharomyces cerevisiae by directed allele replacement technology (DART) screening
Author(s):Bidlingmaier S; Snyder M;
Address:"Department of Molecular, Cellular and Developmental Biology, Yale University, P.O. Box 208103, New Haven, CT 06520-8103, USA"
Journal Title:Funct Integr Genomics
Year:2002
Volume:20011221
Issue:6
Page Number:345 - 356
DOI: 10.1007/s10142-001-0043-1
ISSN/ISBN:1438-793X (Print) 1438-793X (Linking)
Abstract:"In Saccharomyces cerevisiae, apical bud growth occurs for a brief period in G1 when the deposition of membrane and cell wall is restricted to the tip of the growing bud. To identify genes important for apical bud growth, we have utilized a novel transposon-based mutagenesis system termed DART (Directed Allele Replacement Technology) that allows the rapid transfer of defined insertion alleles into any strain background. A total of 4,810 insertion alleles affecting 1,392 different yeast genes were transferred into a cdc34-2 mutant strain that arrests in the apical growth phase when grown at the restrictive temperature of 37 degrees C. We identified 29 insertion alleles, containing mutations in 17 different genes ( SMY1, SPA2, PAN1, SLA1, SLA2, CBK1, SEC22, FAB1, VPS36, VID22, RAS2, ECM33, OPI3, API1/YDR372c, API2/YDR525w, API3/YKR020w, and API4/YNL051w), which alter the elongated bud morphology of cdc34-2 cells arrested in the apical growth phase. Upon treatment with mating pheromone at 25 degrees C, cells containing insertion alleles affecting ten of these genes ( SMY1, SPA2, PAN1, SLA1, SLA2, CBK1, FAB1, VPS36, VID22, and API2/YDR525w) form abnormal mating projections. Additionally, cells containing insertion alleles affecting SEC22, RAS2, API1/YDR372c, API3/YKR020w,and API4/YNL051display severe mating projection formation defects at the elevated temperature of 37 degrees C. DART mutagenesis has many advantages over traditional mutagenesis methods and will be a useful tool for dissecting gene networks important for biological processes"
Keywords:"Alleles Anaphase-Promoting Complex-Cyclosome DNA Transposable Elements/physiology DNA, Fungal/genetics Genes, Fungal/*physiology Ligases/physiology Morphogenesis Mutagenesis, Site-Directed Saccharomyces cerevisiae/*genetics/*growth & development Saccharom;"
Notes:"MedlineBidlingmaier, Scott Snyder, Michael eng GM 36494/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. Germany 2002/04/17 Funct Integr Genomics. 2002 Apr; 1(6):345-56. doi: 10.1007/s10142-001-0043-1. Epub 2001 Dec 21"

 
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