Umeå University's logo

umu.sePublikasjoner
Endre søk
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Variant Polycomb complexes in Drosophila consistent with ancient functional diversity
Division of Genetics, Brigham and Women's Hospital, Boston, United States; Department of Genetics, Harvard Medical School, Boston, United States.
Division of Genetics, Brigham and Women's Hospital, Boston, United States; Department of Genetics, Harvard Medical School, Boston, United States; Biology Department, Emmanuel College, Boston, United States.
Division of Genetics, Brigham and Women's Hospital, Boston, United States; Department of Genetics, Harvard Medical School, Boston, United States.
Division of Genetics, Brigham and Women's Hospital, Boston, United States; Department of Genetics, Harvard Medical School, Boston, United States.
Vise andre og tillknytning
2022 (engelsk)Inngår i: Science Advances, E-ISSN 2375-2548, Vol. 8, nr 36, artikkel-id eadd0103Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Polycomb group (PcG) mutants were first identified in Drosophila on the basis of their failure to maintain proper Hox gene repression during development. The proteins encoded by the corresponding fly genes mainly assemble into one of two discrete Polycomb repressive complexes: PRC1 or PRC2. However, biochemical analyses in mammals have revealed alternative forms of PRC2 and multiple distinct types of noncanonical or variant PRC1. Through a series of proteomic analyses, we identify analogous PRC2 and variant PRC1 complexes in Drosophila, as well as a broader repertoire of interactions implicated in early development. Our data provide strong support for the ancient diversity of PcG complexes and a framework for future analysis in a longstanding and versatile genetic system.

sted, utgiver, år, opplag, sider
NLM (Medline) , 2022. Vol. 8, nr 36, artikkel-id eadd0103
HSV kategori
Identifikatorer
URN: urn:nbn:se:umu:diva-199459DOI: 10.1126/sciadv.add0103ISI: 000911968500040PubMedID: 36070387Scopus ID: 2-s2.0-85137512162OAI: oai:DiVA.org:umu-199459DiVA, id: diva2:1698887
Forskningsfinansiär
NIH (National Institutes of Health), R35-GM126944Swedish Research Council, 2021-04435Tilgjengelig fra: 2022-09-26 Laget: 2022-09-26 Sist oppdatert: 2025-02-07bibliografisk kontrollert

Open Access i DiVA

fulltext(1212 kB)249 nedlastinger
Filinformasjon
Fil FULLTEXT01.pdfFilstørrelse 1212 kBChecksum SHA-512
05cb6ce45a7eb707cb5367ea28af39099509ad7cb9b0f3d0a0aaa04d64b22e15487d9fe77873dcbf47c477549d234382d5acec7e97d01c01ab25ef119710a301
Type fulltextMimetype application/pdf

Andre lenker

Forlagets fulltekstPubMedScopus

Person

Glotov, AlexanderSchwartz, Yuri B.

Søk i DiVA

Av forfatter/redaktør
Glotov, AlexanderSchwartz, Yuri B.
Av organisasjonen
I samme tidsskrift
Science Advances

Søk utenfor DiVA

GoogleGoogle Scholar
Totalt: 249 nedlastinger
Antall nedlastinger er summen av alle nedlastinger av alle fulltekster. Det kan for eksempel være tidligere versjoner som er ikke lenger tilgjengelige

doi
pubmed
urn-nbn

Altmetric

doi
pubmed
urn-nbn
Totalt: 723 treff
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf