Developmental regulation of DNA replication initiation in Drosophila

Developmental gene amplification in the ovarian follicle cells of Drosophila provides a powerful system for the study of metazoan DNA replication. Amplification produces 100kb gradients of amplified DNA through repeated rounds of origin firing and bidirectional movement of replication forks from these origins. The Drosophila Follicle Cell Amplicon at the cytological location 62D, DAFC-62D, is uniquely regulated, with two separate rounds of amplification in developmental stages 10 and 13 of egg chamber development. We investigated mechanisms that control the unusual timing of DAFC-62D origin activation. We first defined origin sequences in DAFC-62D by analyzing the amount of nascent replicative DNA across this amplicon. Surprisingly, the origin coincides with the coding region of a gene named yellow-g2. ORC2 localizes to the origin, as well as two other sites that do not confer origin activity. Both ORC2 and MCM2-7 display differential association with these sequences, corresponding to the two rounds of amplification. All three elements, dispersed in a 7kb central amplified region, are required for either round of DAFC-62D amplification, because deleting any one completely abolished amplification in transposon experiments. Preceded by transcription yellow-g2 in stage 12, the late round of origin firing was ablated by the RNAPII inhibitor a-amanitin. This effect was absent from other amplicons and insulated transposons, and was stage-13 specific for amplification at either the endogenous DAFC-62D or heterologous transposons that did not have functional insulators. Therefore amplification at DAFC-62D in late follicle cell differentiation depends on transcription in cis. Molecularly, blocking RNAPII transcription compromises MCM2-7 recruitment.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Biology.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2007

Author dc:creator

• Xie, Fang, Ph. D. Massachusetts Institute of Technology

Advisor dc:contributor.advisor

• Terry L. Orr-Weaver.

• Biology.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/40862

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/40862