A long noncoding RNA, lincRNA‐Tnfaip3, acts as a coregulator of NF‐κB to modulate inflammatory gene transcription in mouse macrophages. Issue 3 (15th December 2016)
- Record Type:
- Journal Article
- Title:
- A long noncoding RNA, lincRNA‐Tnfaip3, acts as a coregulator of NF‐κB to modulate inflammatory gene transcription in mouse macrophages. Issue 3 (15th December 2016)
- Main Title:
- A long noncoding RNA, lincRNA‐Tnfaip3, acts as a coregulator of NF‐κB to modulate inflammatory gene transcription in mouse macrophages
- Authors:
- Ma, Shibin
Ming, Zhenping
Gong, Ai-Yu
Wang, Yang
Chen, Xiqiang
Hu, Guoku
Zhou, Rui
Shibata, Annemarie
Swanson, Patrick C.
Chen, Xian-Ming - Abstract:
- ABSTRACT: Long intergenic noncoding RNAs (lincRNAs) are long noncoding transcripts (>200 nt) from the intergenic regions of annotated protein‐coding genes. We report here that the lincRNA gene lincRNA‐Tnfaip3, located at mouse chromosome 10 proximal to the tumor necrosis factor α‐induced protein 3 ( Tnfaip3 ) gene, is an early‐primary response gene controlled by nuclear factor‐κB (NF‐κB) signaling in murine macrophages. Functionally, lincRNA‐ Tnfaip3 appears to mediate both the activation and repression of distinct classes of inflammatory genes in macrophages. Specifically, induction of lincRNA‐Tnfaip3 is required for the transactivation of NF‐κB‐regulated inflammatory genes in response to bacterial LPSs stimulation. LincRNA‐Tnfaip3 physically interacts with the high‐mobility group box 1 (Hmgb1), assembling a NF‐κB/Hmgb1/lincRNA‐Tnfaip3 complex in macrophages after LPS stimulation. This resultant NF‐κB/Hmgb1/lincRNA‐Tnfaip3 complex can modulate Hmgb1‐associated histone modifications and, ultimately, transactivation of inflammatory genes in mouse macrophages in response to microbial challenge. Therefore, our data indicate a new regulatory role of NF‐κB‐induced lincRNA‐Tnfaip3 to act as a coactivator of NF‐κB for the transcription of inflammatory genes in innate immune cells through modulation of epigenetic chromatin remodeling.—Ma, S., Ming, Z., Gong, A.‐Y., Wang, Y., Chen, X., Hu, G., Zhou, R., Shibata, A., Swanson, P. C., Chen, X.‐M. A long noncoding RNA, LincRNA‐Tnfaip3,ABSTRACT: Long intergenic noncoding RNAs (lincRNAs) are long noncoding transcripts (>200 nt) from the intergenic regions of annotated protein‐coding genes. We report here that the lincRNA gene lincRNA‐Tnfaip3, located at mouse chromosome 10 proximal to the tumor necrosis factor α‐induced protein 3 ( Tnfaip3 ) gene, is an early‐primary response gene controlled by nuclear factor‐κB (NF‐κB) signaling in murine macrophages. Functionally, lincRNA‐ Tnfaip3 appears to mediate both the activation and repression of distinct classes of inflammatory genes in macrophages. Specifically, induction of lincRNA‐Tnfaip3 is required for the transactivation of NF‐κB‐regulated inflammatory genes in response to bacterial LPSs stimulation. LincRNA‐Tnfaip3 physically interacts with the high‐mobility group box 1 (Hmgb1), assembling a NF‐κB/Hmgb1/lincRNA‐Tnfaip3 complex in macrophages after LPS stimulation. This resultant NF‐κB/Hmgb1/lincRNA‐Tnfaip3 complex can modulate Hmgb1‐associated histone modifications and, ultimately, transactivation of inflammatory genes in mouse macrophages in response to microbial challenge. Therefore, our data indicate a new regulatory role of NF‐κB‐induced lincRNA‐Tnfaip3 to act as a coactivator of NF‐κB for the transcription of inflammatory genes in innate immune cells through modulation of epigenetic chromatin remodeling.—Ma, S., Ming, Z., Gong, A.‐Y., Wang, Y., Chen, X., Hu, G., Zhou, R., Shibata, A., Swanson, P. C., Chen, X.‐M. A long noncoding RNA, LincRNA‐Tnfaip3, acts as a coregulator of NF‐κB to modulate inflammatory gene transcription in mouse macrophages. FASEB J. 31, 1215–1225 (2017). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 31:Issue 3(2017)
- Journal:
- FASEB journal
- Issue:
- Volume 31:Issue 3(2017)
- Issue Display:
- Volume 31, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 31
- Issue:
- 3
- Issue Sort Value:
- 2017-0031-0003-0000
- Page Start:
- 1215
- Page End:
- 1225
- Publication Date:
- 2016-12-15
- Subjects:
- lincRNAs -- Hmgb1 -- inflammation -- histone modifications
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201601056R ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13231.xml