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Article: The PARP1-Siah1 Axis Controls HIV-1 Transcription and Expression of Siah1 Substrates

TitleThe PARP1-Siah1 Axis Controls HIV-1 Transcription and Expression of Siah1 Substrates
Authors
KeywordsE3 ubiquitin ligase Siah1
ELL2
HIV-1 transcription
PARdU
PARP1
PARylation
PARylation-dependent ubiquitination
Poly(ADP-Ribosyl)ation
SEC
super elongation complex
Issue Date2018
Citation
Cell Reports, 2018, v. 23, n. 13, p. 3741-3749 How to Cite?
AbstractYu et al. reveal a critical role for a PARP1-Siah1 axis in controlling HIV-1 viral transcription. The axis increases cellular levels of the transcription factor ELL2 and its associated SEC complex that is required for robust HIV-1 transcription.
Persistent Identifierhttp://hdl.handle.net/10722/324055
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYu, Dan-
dc.contributor.authorLiu, Rongdiao-
dc.contributor.authorYang, Geng-
dc.contributor.authorZhou, Qiang-
dc.date.accessioned2023-01-13T03:01:11Z-
dc.date.available2023-01-13T03:01:11Z-
dc.date.issued2018-
dc.identifier.citationCell Reports, 2018, v. 23, n. 13, p. 3741-3749-
dc.identifier.urihttp://hdl.handle.net/10722/324055-
dc.description.abstractYu et al. reveal a critical role for a PARP1-Siah1 axis in controlling HIV-1 viral transcription. The axis increases cellular levels of the transcription factor ELL2 and its associated SEC complex that is required for robust HIV-1 transcription.-
dc.languageeng-
dc.relation.ispartofCell Reports-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectE3 ubiquitin ligase Siah1-
dc.subjectELL2-
dc.subjectHIV-1 transcription-
dc.subjectPARdU-
dc.subjectPARP1-
dc.subjectPARylation-
dc.subjectPARylation-dependent ubiquitination-
dc.subjectPoly(ADP-Ribosyl)ation-
dc.subjectSEC-
dc.subjectsuper elongation complex-
dc.titleThe PARP1-Siah1 Axis Controls HIV-1 Transcription and Expression of Siah1 Substrates-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1016/j.celrep.2018.05.084-
dc.identifier.pmid29949759-
dc.identifier.pmcidPMC6223328-
dc.identifier.scopuseid_2-s2.0-85048876953-
dc.identifier.volume23-
dc.identifier.issue13-
dc.identifier.spage3741-
dc.identifier.epage3749-
dc.identifier.eissn2211-1247-
dc.identifier.isiWOS:000436517100006-

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