Evidence map›Paper›PMID 23519206›Full record

ArticleFly

A rapidly evolving genomic toolkit for Drosophila heterochromatin.

Mia T Levine, Harmit S Malik

Abstract readComment
In one paragraph

Article in Fly. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. The "life histories" of genes.Journal of molecular evolution · 2015
    Article
  4. Sex chromosome drive.Cold Spring Harbor perspectives in biology · 2014
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Mia T LevineDivision of Basic Sciences; Howard Hughes Medical Institute; Fred Hutchinson Cancer Research Center; Seattle, WA USA.
Harmit S Malik

Funding

Genetic Conflict Shapes Centromeres and HeterochromatinR01GM074108 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MALIK, HARMIT S. · 2005 to 2022
$6.1M
Phylogenomics and functional diversification of the Heterochromatin Protein 1 genF32GM097897 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEVINE, MIA TAUNA · 2011 to 2012
$105k
NIGMS NIH HHS F32 GM097897NIGMS NIH HHS F32-GM097897-02NIGMS NIH HHS R01 GM074108NIGMS NIH HHS R01-GM74108
6 · The paper itself

Abstract

Heterochromatin is the enigmatic eukaryotic genome compartment found mostly at telomeres and centromeres. Conventional approaches to sequence assembly and genetic manipulation fail in this highly repetitive, gene-sparse, and recombinationally silent DNA. In contrast, genetic and molecular analyses of euchromatin-encoded proteins that bind, remodel, and propagate heterochromatin have revealed its vital role in numerous cellular and evolutionary processes. Utilizing the 12 sequenced Drosophila genomes, Levine et al (1) took a phylogenomic approach to discover new such protein "surrogates" of heterochromatin function and evolution. This paper reported over 20 new members of what was traditionally believed to be a small and static Heterochromatin Protein 1 (HP1) gene family. The newly identified HP1 proteins are structurally diverse, lineage-restricted, and expressed primarily in the male germline. The birth and death of HP1 genes follows a "revolving door" pattern, where new HP1s appear to replace old HP1s. Here, we address alternative evolutionary models that drive this constant innovation.

Indexed as

Evolution, MolecularGene ExpressionAnimalsChromosomal Proteins, Non-HistoneDrosophilaDrosophila ProteinsFemaleHeterochromatinMaleChromosomal Proteins, Non-HistoneDrosophila ProteinsHeterochromatinchromodomainchromoshadow domainDrosophilagene duplicationgermlineheterochromatinHeterochromatin Protein 1HP1phylogenomicspseudogenization

Identifiers

PMID23519206
PMCPMC4049844

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.