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Gene Expression

A Sequence-Specific RNA-Binding Protein Complements Apobec-1 To Edit Apolipoprotein B mRNA

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Pages 4426-4432 | Received 18 Mar 1998, Accepted 08 May 1998, Published online: 27 Mar 2023
 

ABSTRACT

The editing of apolipoprotein B (apo-B) mRNA involves the site-specific deamination of cytidine to uracil. The specificity of editing is conferred by an 11-nucleotide mooring sequence located downstream from the editing site. Apobec-1, the catalytic subunit of the editing enzyme, requires additional proteins to edit apo-B mRNA in vitro, but the function of these additional factors, known as complementing activity, is not known. Using RNA affinity chromatography, we show that the complementing activity binds to a 280-nucleotide apo-B RNA in the absence of apobec-1. The activity did not bind to the antisense strand or to an RNA with three mutations in the mooring sequence. The eluate from the wild-type RNA column contained a 65-kDa protein that UV cross-linked to apo-B mRNA but not to the triple-mutant RNA. This protein was not detected in the eluates from the mutant or the antisense RNA columns. Introduction of the mooring sequence into luciferase RNA induced cross-linking of the 65-kDa protein. A 65-kDa protein that interacted with apobec-1 was also detected by far-Western analysis in the eluate from the wild-type RNA column but not from the mutant RNA column. For purification, proteins were precleared on the mutant RNA column prior to chromatography on the wild-type RNA column. Silver staining of the affinity-purified fraction detected a single prominent protein of 65 kDa. Our results suggest that the complementing activity may function as the RNA-binding subunit of the holoenzyme.

ACKNOWLEDGMENTS

This work was supported by NIH grant HL-45478 and an Established Investigator Award from the American Heart Association (D.M.D.). Tissues were obtained from the Regional Primate Research Center at the University of Washington, which is supported by grant RR00166.

We thank Paul Copeland and Shigenori Murata for advice and reading of the manuscript; Bella Gorbatcheva for technical assistance; and Karen Rice, Southwest Foundation for Biomedical Research, for providing tissues.

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