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Apolipoprotein B mRNA editing is an intranuclear event that occurs posttranscriptionally coincident with splicing and
1Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030.
Abstract:
The subcellular compartment in which apolipoprotein (apo) B mRNA is edited is unknown. We studied the site of endogenous apoB mRNA editing and correlated the extent of editing with mRNA maturation in the rat liver. RNA editing activity was demonstrated in both nuclear and cytoplasmic extracts. The specific activity of the editing activity was 5.5-fold higher in the nuclear extract, which was not accounted for by activators, inhibitors, or modulators. However, the total editing activity was 3.1 times higher in the cytoplasmic extract. Highly purified rat liver nuclear apoB mRNA contained 17.3 +/- 1.45% edited sequences compared with 56 +/- 2.5% and 62.15 +/- 6.2% edited sequences in hepatic total and polysomal RNAs, respectively. Because of the significant extent of editing of total nuclear RNA, we fractionated it into a poly(A-) and poly(A+) fraction. While the poly(A-) nuclear fraction contained only 10.4 +/- 1.1% edited sequences, which represents a maximum estimate, the poly(A+) nuclear apoB mRNA contained 50 +/- 1.8% edited sequences, a value very similar to that for polysomal RNA. By direct sequencing of cDNA and genomic clones, we found that as in the case of the human apoB gene, the rat apoB gene contains an intron 25 immediately upstream of the edited exon 26. Using this information, we developed a method to examine in a highly selective manner apoB mRNA that is present in the nucleus before splicing of intron 25 and after splicing of this intron. The unspliced nuclear pre-mRNA contained 7.4 +/- 0.2% edited sequences compared with 51.0 +/- 0.9% edited sequences in the spliced nuclear apoB mRNA. Furthermore, in the poly(A-) pool of apoB pre-mRNA, unspliced nuclear pre-mRNA contained hardly any (1.56%) edited sequences, and the spliced nuclear pre-mRNA contained 7.8 +/- 0.6% edited mRNA. In the poly(A+) fraction, unspliced nuclear pre-mRNA had 25.4 +/- 0.05% and spliced nuclear mRNA 53 +/- 0.6% of its apoB mRNA in an edited form. We conclude that in the rat liver apoB mRNA editing is not a cotransciptional event. It occurs posttranscriptionally, but the process is essentially complete in the spliced polyadenylated apoB mRNA before it leaves the nucleus. Little, if any, additional editing occurs in the cytoplasmic compartment.
Insights
Apolipoprotein B (apoB) mRNA editing occurs post-transcriptionally in rat liver nuclei. Editing is largely complete in spliced, polyadenylated apoB mRNA before it exits the nucleus, with minimal cytoplasmic editing.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- The subcellular location of apolipoprotein (apo) B mRNA editing is not well understood.
- Investigating apoB mRNA editing site and its correlation with mRNA maturation in rat liver is crucial.
Purpose of the Study:
- To determine the subcellular compartment where apoB mRNA editing occurs.
- To correlate apoB mRNA editing extent with mRNA maturation in rat liver.
Main Methods:
- RNA editing activity assays in nuclear and cytoplasmic extracts.
- Fractionation of nuclear RNA into poly(A-) and poly(A+) fractions.
- Selective examination of apoB mRNA before and after intron 25 splicing using cDNA and genomic sequencing.
Main Results:
- Both nuclear and cytoplasmic extracts show RNA editing activity, with higher specific activity in the nucleus.
- Spliced, polyadenylated nuclear apoB mRNA exhibits a high degree of editing (around 50%), similar to polysomal RNA.
- Unspliced nuclear pre-mRNA shows significantly lower editing levels compared to spliced nuclear mRNA.
Conclusions:
- ApoB mRNA editing is a post-transcriptional event in rat liver.
- The editing process is predominantly completed within the nucleus before mRNA export.
- Minimal apoB mRNA editing occurs in the cytoplasmic compartment.