Journal
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
Volume 297, Issue 6, Pages G1181-G1192Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpgi.90636.2008
Keywords
c-myc; liver regeneration; p53
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Funding
- National Institute of Diabetes and Digestive and Kidney Diseases [R01-DK-44649-06, R01-DK-081865-01]
- Medica Foundation [2006-100412]
- National Institute of Drug Abuse Center [DA-011806]
- US Department of Defense Army [W81XWH-07-1-0183]
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Kren BT, Wong PY-P, Shiota A, Zhang X, Zeng Y, Steer CJ. Polysome trafficking of transcripts and microRNAs in regenerating liver after partial hepatectomy. Am J Physiol Gastrointest Liver Physiol 297: G1181-G1192, 2009. First published October 1, 2009; doi: 10.1152/ajpgi.90636.2008.-Liver regeneration after 70% partial hepatectomy (PH) in rats induces > 95% of hepatocytes to undergo two rounds of semisynchronous cell replication. Gene expression is controlled primarily by posttranscriptional processing, including changes in mRNA stability. However, the translational activity of a specific mRNA can also be modulated after PH, resulting in significant uncoupling of protein and transcript levels relative to quiescent liver for many genes including c-myc and p53. Although the precise mechanism by which this uncoupling occurs is unknown, the polysomal association of mRNA and microRNA (miRNA) can significantly modulate rate of decay as well as translational activity. Thus we characterized the association of c-myc and p53 mRNAs and miRNAs in free and cytoskeleton-and membrane-bound polysome populations 3, 6, and 24 h after PH. The transcripts for c-myc and p53 were differentially distributed in the three discrete polysome populations, and this was dramatically modulated during liver regeneration. Nascent polysome-associated p53 and c-myc proteins were also differentially expressed in the free and cytoskeleton-and membrane-bound polysomes and significantly uncoupled from transcript levels relative to nonresected liver. At least 85 miRNAs were associated with the three polysome populations, and their abundance and distribution changed significantly during liver regeneration. These data suggest that posttranscriptional control of c-myc and p53 protein expression is associated with the translocation of transcripts between the different polyribosomes. The alteration of expression for the same transcript in different polysome populations may, in part, be due to the action of miRNAs.
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