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E-GEOD-22018 GSE22018 comparative genomic hybridization by ... Saccharomyces cerevisiae

Loss of DNA replication control is a potent initiator of gene amplification

·发布 2011年5月17日 ·更新 2014年5月2日
406
样本数
203
实验数
1
芯片平台
1
相关文献
实验描述

Eukaryotic cells use numerous mechanisms to ensure that no segment of their DNA is re-replicated within a single cell cycle. Despite longstanding speculation that such tight regulation is needed to protect cells from genomic alterations, this notion has never been experimentally tested. Here we show that even just transient and limited re-replication in Saccharomyces cerevisiae can strongly induce the critical first step of gene amplification, increasing gene copy number from one to two or more. The amplified units, or amplicons, consist of large internal chromosomal segments that are bounded by Ty repetitive elements and are intrachromosomally arrayed at their endogenous locus in direct head-to-tail orientation. The presence of hybrid Ty elements at inter-amplicon junctions together with the dependence of amplification on RAD52 indicate that in budding yeast these re-replication-induced gene amplifications (RRIGA) are mediated by homologous recombination between re-replicated non-allelic repetitive elements. These results finally establish the importance of stringent replication control for genome stability and suggest that re-replication should now be considered as a possible contributor to gene copy number changes in fields as diverse as cancer biology, evolution, and human genetics. The arrays in this series are primary comparative genomic hybridizations to determine genomic changes after re-replication or other genomic stresses. Genomic DNA was purified from reference Saccharomyces cerevisiae cells or survivors of re-replication or other genomic stresses, differentially labeled with Cy3 and Cy5, and competitively hybridized to a spotted microarray containing ORF and intergenic PCR products. Cy5/Cy3 ratios are normalized so that the average ratio of all elements was 1. A small number of the arrays were used to determine the extent and location of re-replication under different conditions. For those, genomic DNA was purified from non-replicating and re-replicating cells and treated as above. Series contains a total of 203 hybridizations.

芯片平台
A-GEOD-3412
Li UCSF yeast 14062 v1.0(203 例)
样本属性
Organism
Saccharomyces cerevisiae
sample type
negative control M ARS317+ 1089 strain in G2/M induced in galactose for 3 h, negative control M ARS317+ 567 strain in G2/M induced in galactose for 3 h, negative control M strain in G2/M, negative control MC2A ars317- 1089 strain in G2/M induced in galactose for 3 h, negative control MC2A ars317- 567 strain in G2/M induced in galactose for 3 h, negative control MC2A strain in G1, negative control MC2A strain in G2/M, negative control strain in G2/M, re-replicating MC2A ARS317+ 1089 strain in G2/M induced in galactose for 3 h, re-replicating MC2A ARS317+ 567 strain in G2/M induced in galactose for 3 h, red sector arising after negative control non-re-replication at ChrIV567, red sector arising after phleomycin treatment, red sector arising after re-replication at ChrIV1089, red sector arising after re-replication at ChrIV567, red sector arising after re-replication at ChrIV567 in dnl4 background, red sector arising after re-replication at ChrIV567 in rad52 background
sector induction
n/a, negative control non-re-replication at ChrIV567, phleomycin treatment, re-replication at ChrIV1089, re-replication at ChrIV567, re-replication at ChrIV567 in dnl4 background, re-replication at ChrIV567 in rad52 background
strain
Sector514, YJL6032, YJL6555, YJL6557, YJL6558, YJL6561, YJL6974, YJL6977, YJL7095, YJL7096, YJL7097, YJL7098, YJL7099, YJL7100, YJL7101, YJL7102, YJL7103, YJL7104, YJL7105, YJL7106, YJL7107, YJL7108, YJL7109, YJL7110, YJL7111, YJL7112, YJL7113, YJL7114, YJL7115, YJL7116, YJL7117, YJL7118, YJL7119, YJL7120, YJL7121, YJL7122, YJL7123, YJL7124, YJL7125, YJL7126, YJL7127, YJL7128, YJL7129, YJL7130, YJL7131, YJL7132, YJL7133, YJL7134, YJL7135, YJL7136, YJL7137, YJL7138, YJL7139, YJL7140, YJL7141, YJL7142, YJL7143, YJL7144, YJL7145, YJL7146, YJL7147, YJL7148, YJL7149, YJL7150, YJL7151, YJL7152, YJL7153, YJL7154, YJL7155, YJL7156, YJL7157, YJL7158, YJL7159, YJL7160, YJL7161, YJL7162, YJL7163, YJL7164, YJL7165, YJL7166, YJL7548, YJL7549, YJL7550, YJL7551, YJL7552, YJL7553, YJL7554, YJL7555, YJL7556, YJL7557, YJL7558, YJL7559, YJL7560, YJL7561, YJL7562, YJL7563, YJL7564, YJL7565, YJL7566, YJL7567, YJL7568, YJL7569, YJL7570, YJL7571, YJL7572, YJL7573, YJL7574, YJL7575, YJL7576, YJL7577, YJL7578, YJL7579, YJL7580, YJL7581, YJL7582, YJL7583, YJL7584, YJL7585, YJL7586, YJL7587, YJL7609, YJL7610, YJL7611, YJL7612, YJL7613, YJL7614, YJL7615, YJL7616, YJL7617, YJL7618, YJL7619, YJL7620, YJL7621, YJL7622, YJL7623, YJL7624, YJL7625, YJL7626, YJL7627, YJL7628, YJL7629, YJL7630, YJL7631, YJL7632, YJL7633, YJL7634, YJL7635, YJL7636, YJL7637, YJL7638, YJL7639, YJL7640, YJL7641, YJL7642, YJL7643, YJL7644, YJL7645, YJL7646, YJL7647, YJL7648, YJL7649, YJL7650, YJL7651, YJL7652, YJL7653, YJL7654, YJL7655, YJL7656, YJL7657, YJL7658, YJL7659, YJL7660, YJL7661, YJL7662, YJL7663, YJL7664, YJL7665, YJL7666, YJL7667, YJL7668, YJL7669, YJL7670, YJL7671, YJL7672, YJL7673, YJL7674, YJL7675, YJL7677, YJL7685, YJL7686, YJL7687, YJL7688, YJL7689, YJL7690, YJL7691, YJL7695
实验信息
登记号
E-GEOD-22018
GEO 编号
GSE22018
实验类型
comparative genomic hybridization by array
物种
Saccharomyces cerevisiae
发布日期
2011年5月17日
更新日期
2014年5月2日
提交者
Kenneth J Finn、 Joachim J Li、 Brian M Green、 Brian M Green
分析服务
分析服务

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