ORC localization in Drosophila follicle cells and the effects of mutations in dE2F and dDP. - Wikidata - wikimedia - TriplyDB

ORC localization in Drosophila follicle cells and the effects of mutations in dE2F and dDP.

ORC localization in Drosophila follicle cells and the effects of mutations in dE2F and dDP.

http://www.wikidata.org/entity/Q35193528

about

Mre11 complex and DNA replication: linkage to E2F and sites of DNA synthesis A WD-repeat protein stabilizes ORC binding to chromatin Functional analysis of mutant and wild-type Drosophila origin recognition complex Drosophila double parked: a conserved, essential replication protein that colocalizes with the origin recognition complex and links DNA replication with mitosis and the down-regulation of S phase transcripts The anaphase-promoting complex/cyclosome (APC/C) is required for rereplication control in endoreplication cycles Regulation of E2F1 by BRCT domain-containing protein TopBP1 Retinoblastoma family genes The human origin recognition complex protein 1 dissociates from chromatin during S phase in HeLa cells Mammalian MCM loading in late-G(1) coincides with Rb hyperphosphorylation and the transition to post-transcriptional control of progression into S-phase The N Terminus of the Retinoblastoma Protein Inhibits DNA Replication via a Bipartite Mechanism Disrupted in Partially Penetrant Retinoblastomas.Cell size checkpoint control by the retinoblastoma tumor suppressor pathway The carnegie protein trap library: a versatile tool for Drosophila developmental studies.Arabidopsis E2FA stimulates proliferation and endocycle separately through RBR-bound and RBR-free complexes.The N-terminal domain of the Drosophila retinoblastoma protein Rbf1 interacts with ORC and associates with chromatin in an E2F independent manner Cell cycle arrest by transforming growth factor beta1 near G1/S is mediated by acute abrogation of prereplication complex activation involving an Rb-MCM interaction.Drosophila ORC localizes to open chromatin and marks sites of cohesin complex loading Interaction of the retinoblastoma protein with Orc1 and its recruitment to human origins of DNA replication.Analysis of Cell Cycle Switches in Drosophila Oogenesis.Localisation of the DmCdc45 DNA replication factor in the mitotic cycle and during chorion gene amplification E2F mediates developmental and cell cycle regulation of ORC1 in Drosophila.Drosophila minichromosome maintenance 6 is required for chorion gene amplification and genomic replication.The anaphase promoting complex/cyclosome is required during development for modified cell cycles.dREAM co-operates with insulator-binding proteins and regulates expression at divergently paired genes.In search of the holy replicator Drosophila cyclin E interacts with components of the Brahma complex Tumor suppression by a severely truncated species of retinoblastoma protein.Spotted-dick, a zinc-finger protein of Drosophila required for expression of Orc4 and S phase S phase-coupled E2f1 destruction ensures homeostasis in proliferating tissues.Precocious S-phase entry in budding yeast prolongs replicative state and increases dependence upon Rad53 for viability.Transcriptional repressor functions of Drosophila E2F1 and E2F2 cooperate to inhibit genomic DNA synthesis in ovarian follicle cells.Functionally distinct, sequence-specific replicator and origin elements are required for Drosophila chorion gene amplification Functional antagonism between E2F family members Characterization of a novel origin recognition complex-like complex: implications for DNA recognition, cell cycle control, and locus-specific gene amplification Drosophila ORC specifically binds to ACE3, an origin of DNA replication control element RBF and Rno promote photoreceptor differentiation onset through modulating EGFR signaling in the Drosophila developing eye Safeguarding genetic information in Drosophila.Analysis of model replication origins in Drosophila reveals new aspects of the chromatin landscape and its relationship to origin activity and the prereplicative complex The cyclin-dependent kinase inhibitor Dacapo promotes replication licensing during Drosophila endocycles.Drosophila follicle cell amplicons as models for metazoan DNA replication: a cyclinE mutant exhibits increased replication fork elongation DNA sequence templates adjacent nucleosome and ORC sites at gene amplification origins in Drosophila.

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P2860

ORC localization in Drosophila follicle cells and the effects of mutations in dE2F and dDP.

http://www.wikidata.org/entity/Q35193528

description

1999 nî lūn-bûn

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1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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1999 թվականի ապրիլին հրատարակված գիտական հոդված

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1999年の論文

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1999年学术文章

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1999年学术文章

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1999年学术文章

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1999年学术文章

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1999年学术文章

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1999年學術文章

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name

ORC localization in Drosophila ...... of mutations in dE2F and dDP.

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ORC localization in Drosophila ...... of mutations in dE2F and dDP.

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type

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ORC localization in Drosophila ...... of mutations in dE2F and dDP.

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ORC localization in Drosophila ...... of mutations in dE2F and dDP.

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prefLabel

ORC localization in Drosophila ...... of mutations in dE2F and dDP.

@ast

ORC localization in Drosophila ...... of mutations in dE2F and dDP.

@en

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ORC localization in Drosophila ...... of mutations in dE2F and dDP.

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G Bosco

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I Royzman

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R J Austin

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S P Bell

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P2860

E2F-6, a member of the E2F family that can behave as a transcriptional repressor

Heterodimerization of the transcription factors E2F-1 and DP-1 leads to cooperative trans-activation

Mutations of the Drosophila dDP, dE2F, and cyclin E genes reveal distinct roles for the E2F-DP transcription factor and cyclin E during the G1-S transition.

Expression of the HsOrc1 gene, a human ORC1 homolog, is regulated by cell proliferation via the E2F transcription factor

Chromosome association of minichromosome maintenance proteins in Drosophila endoreplication cycles

The retinoblastoma protein and cell cycle control

Components and dynamics of DNA replication complexes in S. cerevisiae: redistribution of MCM proteins and Cdc45p during S phase

Initiation of DNA replication in eukaryotic cells

Retinoblastoma protein recruits histone deacetylase to repress transcription

Retinoblastoma protein represses transcription by recruiting a histone deacetylase

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