Polyadenylation is dispensable for encapsidation and reverse transcription of hepatitis B viral pregenomic RNA

Hye Jin Lee, Jehan Lee, Myeong Kyun Shin, Wang Shick Ryu

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

A hepadnaviruses replicates its DNA genome via reverse transcription of an RNA template (pregenomic RNA or pgRNA), which has a cap structure at the 5′ end and a poly(A) tail at the 3′ end. We have previously shown that the 5′ cap is indispensable for encapsidation of the pgRNA. A speculative extension of the above finding is that the cap contributes to encapsidation via its interaction with the poly(A) tail, possibly involving eIF4E-eIF4G-PABP interaction. To test this hypothesis, poly(A)-less pgRNAs were generated via cleavage by a cis-acting hepatitis delta virus ribozyme sequence. We found that accumulation of the poly(A)-less pgRNA was markedly diminished, mostly likely due to its reduced stability. Importantly, however, the remaining poly(A)-less pgRNAs were nonetheless encapsidated and reverse transcribed normally when the reduced stability was taken account. Our finding clearly contradicts the notion that the poly(A) tail has any function in encapsidation and viral reverse transcription.

Original languageEnglish
Pages (from-to)545-552
Number of pages8
JournalMolecules and cells
Volume25
Issue number4
Publication statusPublished - 2008 Jun 30

Fingerprint

Polyadenylation
Poly A
Viral RNA
Hepatitis B
Reverse Transcription
Messenger RNA
Hepadnaviridae
RNA
Hepatitis Delta Virus
Catalytic RNA
Genome
DNA
pgRNA

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Cell Biology

Cite this

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Polyadenylation is dispensable for encapsidation and reverse transcription of hepatitis B viral pregenomic RNA. / Lee, Hye Jin; Lee, Jehan; Shin, Myeong Kyun; Ryu, Wang Shick.

In: Molecules and cells, Vol. 25, No. 4, 30.06.2008, p. 545-552.

Research output: Contribution to journalArticle

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