4.4 Article

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

期刊

RNA
卷 17, 期 1, 页码 39-44

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.2252511

关键词

RNA terminal nucleotidyl transferase; hydroxyurea; inhibition of DNA replication; mRNA turnover

资金

  1. Cancer Research UK
  2. Biotechnology and Biological Sciences Research Council
  3. EP Abraham Research Fund
  4. Wellcome Trust
  5. Biotechnology and Biological Sciences Research Council [BB/F013531/1] Funding Source: researchfish
  6. BBSRC [BB/F013531/1] Funding Source: UKRI

向作者/读者索取更多资源

Inhibition of eukaryotic DNA replication leads to the rapid suppression of histone synthesis, via 39 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.

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