The human cytoplasmic RNA terminal U-transferase ZCCHC11 targets histone mRNAs for degradation.

Journal article

Inhibition of eukaryotic DNA replication leads to the rapid suppression of histone synthesis, via 3' uridylation of cytoplasmic histone mRNAs followed by their Lsm1-7-mediated decapping and degradation. Here we show that the human cytoplasmic RNA terminal U-transferase ZCCHC11, recently implicated in microRNA metabolism, associates with replication-dependent histone mRNAs. Knockdown of ZCCHC11 selectively blocked histone mRNA degradation following inhibition of DNA replication, whereas knockdown of PAPD1 or PAPD5, previously proposed as candidate histone mRNA U-transferases, had no such effect. Furthermore, a reduction in the proportion of histone transcripts that were uridylated was observed following ZCCHC11 knockdown. Our data indicate that ZCCHC11 is the terminal U-transferase responsible for targeting human histone mRNAs for degradation following inhibition or completion of DNA replication.

Authors: Schmidt, M; West, S; Norbury, C

• Publication status: Published
• Journal: RNA (New York, N.Y.)
• Volume: 17
• Issue: 1
• Pages: 39-44
• Publication date: 2011-01-01
• DOI: 10.1261/rna.2252511
• EISSN: 1469-9001
• ISSN: 1355-8382
• Language: English
• Keywords: RNA; RNA 3' End Processing; Blotting, Western; Immunoprecipitation; Humans; Kidney; Hela Cells; RNA Stability; RNA, Small Interfering; Reverse Transcriptase Polymerase Chain Reaction; Histones; Cytoplasm; Cells, Cultured; DNA Replication; RNA, Messenger; DNA-Binding Proteins