Redox regulation of a novel L1Md-A2 retrotransposon in vascular smooth muscle cells

Kim P. Lu, Kenneth Ramos

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Activation and reintegration of retrotransposons into the genome is linked to several diseases in human and rodents, but mechanisms of gene activation remain largely unknown. Here we identify a novel gene of L1Md-A2 lineage in vascular smooth muscle cells and show that environmental hydrocarbons enhance gene expression and activate monomer-driven transcription via a redox-sensitive mechanism. Site-directed mutagenesis and progressive deletion analyses identified two antioxidant/electrophile response-like elements (5′-GTGACTCGAGC-3′) within the A2/3 and A3 region. These elements mediated activation, with the A3 monomer playing an essential role in transactivation. This signaling pathway may contribute to gene instability during the course of atherogenesis.

Original languageEnglish (US)
Pages (from-to)28201-28209
Number of pages9
JournalJournal of Biological Chemistry
Volume278
Issue number30
DOIs
StatePublished - Jul 25 2003
Externally publishedYes

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Retroelements
Vascular Smooth Muscle
varespladib methyl
Transcriptional Activation
Oxidation-Reduction
Smooth Muscle Myocytes
Muscle
Genes
Cells
Antioxidant Response Elements
Chemical activation
Hydrocarbons
Site-Directed Mutagenesis
Rodentia
Atherosclerosis
Antioxidants
Monomers
Genome
Gene Expression
Mutagenesis

ASJC Scopus subject areas

  • Biochemistry

Cite this

Redox regulation of a novel L1Md-A2 retrotransposon in vascular smooth muscle cells. / Lu, Kim P.; Ramos, Kenneth.

In: Journal of Biological Chemistry, Vol. 278, No. 30, 25.07.2003, p. 28201-28209.

Research output: Contribution to journalArticle

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