4.8 Article

Regulation of the Apolipoprotein Gene Cluster by a Long Noncoding RNA

Journal

CELL REPORTS
Volume 6, Issue 1, Pages 222-230

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2013.12.015

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Funding

  1. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH083733, R01MH084880] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS063974] Funding Source: NIH RePORTER
  3. NIMH NIH HHS [R01 MH083733, R01 MH084880] Funding Source: Medline
  4. NINDS NIH HHS [R01 NS063974] Funding Source: Medline

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Apolipoprotein A1 (APOA1) is the major protein component of high-density lipoprotein (HDL) in plasma. We have identified an endogenously expressed long noncoding natural antisense transcript, APOA1-AS, which acts as a negative transcriptional regulator of APOA1 both in vitro and in vivo. Inhibition of APOA1-AS in cultured cells resulted in the increased expression of APOA1 and two neighboring genes in the APO cluster. Chromatin immunoprecipitation (ChIP) analyses of a similar to 50 kb chromatin region flanking the APOA1 gene demonstrated that APOA1-AS can modulate distinct histone methylation patterns that mark active and/or inactive gene expression through the recruitment of histone-modifying enzymes. Targeting APOA1-AS with short antisense oligonucleotides also enhanced APOA1 expression in both human and monkey liver cells and induced an increase in hepatic RNA and protein expression in African green monkeys. Furthermore, the results presented here highlight the significant local modulatory effects of long noncoding antisense RNAs and demonstrate the therapeutic potential of manipulating the expression of these transcripts both in vitro and in vivo.

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