Evidence map›Paper›PMID 30384843›Full record

ArticleEpigenetics & chromatin2018

The large fraction of heterochromatin in Drosophila neurons is bound by both B-type lamin and HP1a.

Alexey V Pindyurin, Artem A Ilyin, Anton V Ivankin, Mikhail V Tselebrovsky, Valentina V Nenasheva, Elena A Mikhaleva, Ludo Pagie, Bas van Steensel, Yuri Y Shevelyov

Open access · goldAbstract read
In one paragraph

Article in Epigenetics & chromatin, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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

26 citing papers in PubMed, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Alexey V PindyurinDivision of Gene Regulation, Netherlands Cancer Institute, 1066 CX, Amsterdam, The Netherlands. a.pindyurin@mcb.nsc.ru.
Artem A IlyinDepartment of Molecular Genetics of Cell, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia, 123182.
Anton V IvankinDepartment of Regulation of Genetic Processes, Institute of Molecular and Cellular Biology, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia, 630090.
Mikhail V TselebrovskyDepartment of Molecular Genetics of Cell, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia, 123182.
Valentina V NenashevaDepartment of Viral and Cellular Molecular Genetics, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia, 123182.
Elena A MikhalevaDepartment of Molecular Genetics of Cell, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia, 123182.
Ludo PagieDivision of Gene Regulation, Netherlands Cancer Institute, 1066 CX, Amsterdam, The Netherlands.
Bas van SteenselDivision of Gene Regulation, Netherlands Cancer Institute, 1066 CX, Amsterdam, The Netherlands.
Yuri Y ShevelyovDepartment of Molecular Genetics of Cell, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia, 123182. shevelev@img.ras.ru.ORCID 0000-0002-0568-9236
Institute of Molecular Genetics · RURussian Academy of Sciences · RUErasmus MC · NLThe Netherlands Cancer Institute · NLYaroslavl State Medical Academy · RU

Funding

European Research Council 293662
6 · The paper itself

Abstract

backgroundIn most mammalian cell lines, chromatin located at the nuclear periphery is represented by condensed heterochromatin, as evidenced by microscopy observations and DamID mapping of lamina-associated domains (LADs) enriched in dimethylated Lys9 of histone H3 (H3K9me2). However, in Kc167 cell culture, the only Drosophilla cell type where LADs have previously been mapped, they are neither H3K9me2-enriched nor overlapped with the domains of heterochromatin protein 1a (HP1a).

resultsHere, using cell type-specific DamID we mapped genome-wide LADs, HP1a and Polycomb (Pc) domains from the central brain, Repo-positive glia, Elav-positive neurons and the fat body of Drosophila third instar larvae. Strikingly, contrary to Kc167 cells of embryonic origin, in neurons and, to a lesser extent, in glia and the fat body, HP1a domains appear to overlap strongly with LADs in both the chromosome arms and pericentromeric regions. Accordingly, centromeres reside closer to the nuclear lamina in neurons than in Kc167 cells. As expected, active gene promoters are mostly not present in LADs, HP1a and Pc domains. These domains are occupied by silent or weakly expressed genes with genes residing in the HP1a-bound LADs expressed at the lowest level.

conclusionsIn various differentiated Drosophila cell types, we discovered the existence of peripheral heterochromatin, similar to that observed in mammals. Our findings support the model that peripheral heterochromatin matures enhancing the repression of unwanted genes as cells terminally differentiate.

Indexed as

AnimalsCell LineChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneDrosophilaDrosophila ProteinsHeterochromatinHistonesLamin Type BNeuronsProtein BindingChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneDrosophila ProteinsHeterochromatinHistonesLamin Type BB-type laminDrosophilaHeterochromatinHP1Lamina-associated domainsPolycomb

Identifiers

PMID30384843
PMCPMC6211408
OpenAlexW2898784229

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LicenceCC BY
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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.