Developmental control of the DNA replication and transcription programs

被引:66
|
作者
Nordman, Jared [1 ,2 ]
Li, Sharon [1 ,2 ]
Eng, Thomas [1 ,2 ]
MacAlpine, David [3 ]
Orr-Weaver, Terry L. [1 ,2 ]
机构
[1] MIT, Whitehead Inst, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
关键词
DROSOPHILA-MELANOGASTER; GENE AMPLIFICATION; CELL-CYCLE; FAT-BODY; LARVAL; EXPRESSION; TISSUE; POLYPLOIDY; TARGETS; PROFILE;
D O I
10.1101/gr.114611.110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polyploid or polytene cells, which have more than 2C DNA content, are widespread throughout nature and present in most differentiated Drosophila tissues. These cells also can display differential replication, that is, genomic regions of increased or decreased DNA copy number relative to overall genomic ploidy. How frequently differential replication is used as a developmental strategy remains unclear. Here, we use genome-wide array-based comparative genomic hybridization (aCGH) to profile differential DNA replication in isolated and purified larval fat body and midgut tissues of Drosophila, and we compare them with recent aCGH profiles of the larval salivary gland. We identify sites of euchromatic underreplication that are common to all three tissues and others that are tissue specific. We demonstrate that both common and tissue-specific underreplicated sites are dependent on the Suppressor of Underreplication protein, SUUR. mRNA-seq profiling shows that whereas underreplicated regions are generally transcriptionally silent in the larval midgut and salivary gland, transcriptional silencing and underreplication have been uncoupled in the larval fat body. In addition to revealing the prevalence of differential replication, our results show that transcriptional silencing and underreplication can be mechanistically uncoupled.
引用
收藏
页码:175 / 181
页数:7
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