On the public citation graph
Insulator proteins contribute to expression of gene loci repositioned into heterochromatin in the course of Drosophila evolution
0 signed · 98 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-62703-646-7_6openalex-snapshot
Clustal Omega, Accurate Alignment of Very Large Numbers of Sequences
inferredcites →https://doi.org/10.1007/bf00135277openalex-snapshot
Cytological and linkage maps of Drosophila virilis chromosomes
inferredcites →https://doi.org/10.1007/s004120050389openalex-snapshot
Evidence for an antagonistic relationship between the boundary element-associated factor BEAF and the transcription factor DREF
inferredcites →https://doi.org/10.1016/j.bbagrm.2007.11.011openalex-snapshot
The DRE/DREF transcriptional regulatory system: a master key for cell proliferation
inferredcites →https://doi.org/10.1016/j.cell.2010.09.009openalex-snapshot
Systematic Protein Location Mapping Reveals Five Principal Chromatin Types in Drosophila Cells
inferredcites →https://doi.org/10.1016/j.devcel.2008.02.002openalex-snapshot
Intron Delays and Transcriptional Timing during Development
inferredcites →https://doi.org/10.1016/j.febslet.2013.10.039openalex-snapshot
Chromatin insulators and long‐distance interactions in Drosophila
inferredcites →https://doi.org/10.1016/j.molcel.2005.09.002openalex-snapshot
Antisense Transcription and Heterochromatin at the DM1 CTG Repeats Are Constrained by CTCF
inferredcites →https://doi.org/10.1016/j.molcel.2013.04.018openalex-snapshot
Chromatin Insulators: Linking Genome Organization to Cellular Function
inferredcites →https://doi.org/10.1016/j.plantsci.2015.04.017openalex-snapshot
The enduring mystery of intron-mediated enhancement
inferredcites →https://doi.org/10.1016/j.tcb.2014.08.003openalex-snapshot
Architectural proteins: regulators of 3D genome organization in cell fate
inferredcites →https://doi.org/10.1016/j.tig.2006.04.008openalex-snapshot
Oxymoron no more: the expanding world of heterochromatic genes
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1016/s0378-1119(02)00890-9openalex-snapshot
The DNA replication-related element-binding factor (DREF) is a transcriptional regulator of the Drosophila myb gene
inferredcites →https://doi.org/10.1016/s0378-1119(03)00493-1openalex-snapshot
Transcription control of a gene for Drosophila transcription factor, DREF by DRE and cis-elements conserved between Drosophila melanogaster and virilis
inferredcites →https://doi.org/10.1016/s0960-9822(03)00558-xopenalex-snapshot
Remarkable Interkingdom Conservation of Intron Positions and Massive, Lineage-Specific Intron Loss and Gain in Eukaryotic Evolution
inferredcites →https://doi.org/10.1016/s1937-6448(08)01801-7openalex-snapshot
Chapter 1 Cellular Mechanism for Targeting Heterochromatin Formation in Drosophila
inferredcites →https://doi.org/10.1038/nature05915openalex-snapshot
The complex language of chromatin regulation during transcription
inferredcites →https://doi.org/10.1038/nature06341openalex-snapshot
Evolution of genes and genomes on the Drosophila phylogeny
inferredcites →https://doi.org/10.1038/ncb1580openalex-snapshot
Loss of Drosophila Myb interrupts the progression of chromosome condensation
inferredcites →https://doi.org/10.1038/ng940openalex-snapshot
Selection for short introns in highly expressed genes
inferredcites →https://doi.org/10.1038/nrm3941openalex-snapshot
Histone exchange, chromatin structure and the regulation of transcription
inferredcites →https://doi.org/10.1038/nsmb.1659openalex-snapshot
Chromatin organization marks exon-intron structure
inferredcites →https://doi.org/10.1038/s41467-017-02525-wopenalex-snapshot
High-resolution TADs reveal DNA sequences underlying genome organization in flies
inferredcites →https://doi.org/10.1038/s41598-017-04476-0openalex-snapshot
Identification of introns harboring functional sequence elements through positional conservation
inferredcites →https://doi.org/10.1073/pnas.0503424102openalex-snapshot
Evolution of heterochromatic genes of Drosophila
inferredcites →https://doi.org/10.1073/pnas.0509063102openalex-snapshot
Occupancy of the Drosophila hsp70 promoter by a subset of basal transcription factors diminishes upon transcriptional activation
inferredcites →https://doi.org/10.1073/pnas.0800250105openalex-snapshot
Splicing promotes rapid and efficient mRNA export in mammalian cells
inferredcites →https://doi.org/10.1073/pnas.1207036109openalex-snapshot
Ectopic assembly of heterochromatin in Drosophila melanogaster triggered by transposable elements
inferredcites →https://doi.org/10.1073/pnas.92.9.3804openalex-snapshot
Transposable elements are stable structural components of Drosophila melanogaster heterochromatin.
inferredcites →https://doi.org/10.1080/19336934.2016.1225634openalex-snapshot
Trans-inactivation: Repression in a wrong place
inferredcites →https://doi.org/10.1089/cmb.1994.1.39openalex-snapshot
QGB: Combined Use of Sequence Similarity and Codon Bias for Coding Region Identification
inferredcites →https://doi.org/10.1093/bib/3.3.265openalex-snapshot
PROSITE: A documented database using patterns and profiles as motif descriptors
inferredcites →https://doi.org/10.1093/bib/bbs017openalex-snapshot
Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
inferredcites →https://doi.org/10.1093/bioinformatics/btp033openalex-snapshot
Jalview Version 2—a multiple sequence alignment editor and analysis workbench
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btu808openalex-snapshot
Kablammo: an interactive, web-based BLAST results visualizer
inferredcites →https://doi.org/10.1093/emboj/21.4.675openalex-snapshot
Myb controls G2/M progression by inducing cyclin B expression in the Drosophila eye imaginal disc
inferredcites →https://doi.org/10.1093/genetics/125.1.141openalex-snapshot
The effects of chromosome rearrangements on the expression of heterochromatic genes in chromosome 2L of Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/127.3.553openalex-snapshot
Cytogenetic analysis of the second chromosome heterochromatin of Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/128.4.785openalex-snapshot
The effect of modifiers of position-effect variegation on the variegation of heterochromatic genes of Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/134.1.277openalex-snapshot
The role of heterochromatin in the expression of a heterochromatic gene, the rolled locus of Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/140.3.1033openalex-snapshot
Cis-effects of heterochromatin on heterochromatic and euchromatic gene activity in Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/155.2.699openalex-snapshot
Heterochromatin Protein 1 Is Required for the Normal Expression of Two Heterochromatin Genes in Drosophila
inferredcites →https://doi.org/10.1093/molbev/msm088openalex-snapshot
PAML 4: Phylogenetic Analysis by Maximum Likelihood
inferredcites →https://doi.org/10.1093/molbev/msu226openalex-snapshot
Transcript Length Mediates Developmental Timing of Gene Expression Across Drosophila
inferredcites →https://doi.org/10.1093/molbev/msy096openalex-snapshot
MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1093/nar/gkl315openalex-snapshot
PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments
inferredcites →https://doi.org/10.1093/nar/gkp335openalex-snapshot
MEME SUITE: tools for motif discovery and searching
inferredcites →https://doi.org/10.1093/nar/gks1067openalex-snapshot
New and continuing developments at PROSITE
inferredcites →https://doi.org/10.1093/nar/gkt1165openalex-snapshot
OnTheFly: a database of Drosophila melanogaster transcription factors and their binding sites
inferredcites →https://doi.org/10.1093/nar/gkt158openalex-snapshot
HP1a, Su(var)3-9, SETDB1 and POF stimulate or repress gene expression depending on genomic position, gene length and expression pattern in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/nar/gku365openalex-snapshot
deepTools: a flexible platform for exploring deep-sequencing data
inferredcites →https://doi.org/10.1093/nar/gkw371openalex-snapshot
Architectural proteins Pita, Zw5,and ZIPIC contain homodimerization domain and support specific long-range interactions inDrosophila
inferredcites →https://doi.org/10.1093/nar/gky957openalex-snapshot
REDfly: the transcriptional regulatory element database for Drosophila
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040023openalex-snapshot
Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees.
inferredcites →https://doi.org/10.1101/cshperspect.a017780openalex-snapshot
Position-Effect Variegation, Heterochromatin Formation, and Gene Silencing in Drosophila
inferredcites →https://doi.org/10.1101/gad.12.18.2852openalex-snapshot
Loss of transcriptional activity of a transgene is accompanied by DNA methylation and histone deacetylation and is prevented by insulators
inferredcites →https://doi.org/10.1101/gad.1643208openalex-snapshot
NELF-mediated stalling of Pol II can enhance gene expression by blocking promoter-proximal nucleosome assembly
inferredcites →https://doi.org/10.1101/gad.1798209openalex-snapshot
Three subclasses of a Drosophila insulator show distinct and cell type-specific genomic distributions
inferredcites →https://doi.org/10.1101/gr.092759.109openalex-snapshot
Circos: An information aesthetic for comparative genomics
inferredcites →https://doi.org/10.1101/gr.110098.110openalex-snapshot
Plasticity in patterns of histone modifications and chromosomal proteins in Drosophila heterochromatin
inferredcites →https://doi.org/10.1101/gr.138156.112openalex-snapshot
Nature and function of insulator protein binding sites in the Drosophila genome
inferredcites →https://doi.org/10.1101/gr.174169.114openalex-snapshot
Two new insulator proteins, Pita and ZIPIC, target CP190 to chromatin
inferredcites →https://doi.org/10.1101/sqb.2010.75.039openalex-snapshot
Drosophila Heat Shock System as a General Model to Investigate Transcriptional Regulation
inferredcites →https://doi.org/10.1105/tpc.17.00020openalex-snapshot
Intron DNA Sequences Can Be More Important Than the Proximal Promoter in Determining the Site of Transcript Initiation
inferredcites →https://doi.org/10.1128/mcb.01748-08openalex-snapshot
Genome-Wide Mapping of Boundary Element-Associated Factor (BEAF) Binding Sites in Drosophila melanogaster Links BEAF to Transcription
inferredcites →https://doi.org/10.1186/1471-2148-7-192openalex-snapshot
Patterns of intron gain and conservation in eukaryotic genes
inferredcites →https://doi.org/10.1186/1471-2148-7-87openalex-snapshot
Molecular phylogeny of the Drosophila obscura species group, with emphasis on the Old World species
inferredcites →https://doi.org/10.1186/gb-2007-8-2-r24openalex-snapshot
Quantifying similarity between motifs
inferredcites →https://doi.org/10.1186/gb-2008-9-9-r137openalex-snapshot
Model-based Analysis of ChIP-Seq (MACS)
inferredcites →https://doi.org/10.1186/gb-2009-10-3-r25openalex-snapshot
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
inferredcites →https://doi.org/10.1242/jeb.143008openalex-snapshot
Phylogeny, environment and sexual communication across the Drosophila genus
inferredcites →https://doi.org/10.1242/jeb.204.13.2331openalex-snapshot
Evolution of water balance in the genusDrosophila
inferredcites →https://doi.org/10.1261/rna.5250403openalex-snapshot
A quantitative analysis of intron effects on mammalian gene expression
inferredcites →https://doi.org/10.1371/journal.pbio.0050152openalex-snapshot
Principles of Genome Evolution in the Drosophila melanogaster Species Group
inferredcites →https://doi.org/10.1371/journal.pcbi.0010043openalex-snapshot
ReAS: Recovery of Ancestral Sequences for Transposable Elements from the Unassembled Reads of a Whole Genome Shotgun
inferredcites →https://doi.org/10.1371/journal.pgen.0030038openalex-snapshot
High-Resolution Mapping Reveals Links of HP1 with Active and Inactive Chromatin Components
inferredcites →https://doi.org/10.1371/journal.pgen.0040016openalex-snapshot
Molecular Landscape of Modified Histones in Drosophila Heterochromatic Genes and Euchromatin-Heterochromatin Transition Zones
inferredcites →https://doi.org/10.1371/journal.pgen.1000453openalex-snapshot
The Impact of Local Genome Sequence on Defining Heterochromatin Domains
inferredcites →https://doi.org/10.1371/journal.pgen.1002954openalex-snapshot
Enrichment of HP1a on Drosophila Chromosome 4 Genes Creates an Alternate Chromatin Structure Critical for Regulation in this Heterochromatic Domain
inferredcites →https://doi.org/10.1371/journal.pgen.1003061openalex-snapshot
HP1a Recruitment to Promoters Is Independent of H3K9 Methylation in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1006212openalex-snapshot
Comparative Genomic Analyses Provide New Insights into the Evolutionary Dynamics of Heterochromatin in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0012339openalex-snapshot
Complex Exon-Intron Marking by Histone Modifications Is Not Determined Solely by Nucleosome Distribution
inferredcites →https://doi.org/10.1371/journal.pone.0113010openalex-snapshot
On the Evolution of Yeti, a Drosophila melanogaster Heterochromatin Gene
inferredcites →https://doi.org/10.1371/journal.pone.0173602openalex-snapshot
The GAGA factor regulatory network: Identification of GAGA factor associated proteins
inferredcites →https://doi.org/10.1371/journal.pone.0203843openalex-snapshot
4C-seq characterization of Drosophila BEAF binding regions provides evidence for highly variable long-distance interactions between active chromatin
inferredcites →https://doi.org/10.1534/g3.119.0003openalex-snapshot
Genetic and Molecular Analysis of Essential Genes in Centromeric Heterochromatin of the Left Arm of Chromosome 3 inDrosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.106.056069openalex-snapshot
Heterochromatic Genes in Drosophila: A Comparative Analysis of Two Genes
inferredcites →https://doi.org/10.1534/genetics.107.086074openalex-snapshot
Polytene Chromosomal Maps of 11 Drosophila Species: The Order of Genomic Scaffolds Inferred From Genetic and Physical Maps
inferredcites →https://doi.org/10.1534/genetics.107.086108openalex-snapshot
Chromosomal Rearrangement Inferred From Comparisons of 12 Drosophila Genomes
inferredcites →https://doi.org/10.1534/genetics.110.117259openalex-snapshot
Essential Loci in Centromeric Heterochromatin of Drosophila melanogaster. I: The Right Arm of Chromosome 2
inferredcites →https://doi.org/10.1534/genetics.115.181693openalex-snapshot
The Differences BetweenCis- andTrans-Gene Inactivation Caused by Heterochromatin inDrosophila
inferredcites →https://doi.org/10.1534/genetics.117.300583openalex-snapshot
Phylogeny of the Genus Drosophila
inferredcites →https://doi.org/10.3389/fgene.2014.00028openalex-snapshot
Mechanisms and proteins involved in long-distance interactions
inferredcites →https://doi.org/10.4161/cc.24742openalex-snapshot
Dynamic changes in the genomic localization of DNA replication-related element binding factor during the cell cycle
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1186/s13100-020-0205-0openalex-snapshot
Hybrid dysgenesis in Drosophila virilis results in clusters of mitotic recombination and loss-of-heterozygosity but leaves meiotic recombination unaltered
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.