Genomewide characterization of non-polyadenylated RNAs

Genome Biol. 2011;12(2):R16. doi: 10.1186/gb-2011-12-2-r16. Epub 2011 Feb 16.

Abstract

Background: RNAs can be physically classified into poly(A)+ or poly(A)- transcripts according to the presence or absence of a poly(A) tail at their 3' ends. Current deep sequencing approaches largely depend on the enrichment of transcripts with a poly(A) tail, and therefore offer little insight into the nature and expression of transcripts that lack poly(A) tails.

Results: We have used deep sequencing to explore the repertoire of both poly(A)+ and poly(A)- RNAs from HeLa cells and H9 human embryonic stem cells (hESCs). Using stringent criteria, we found that while the majority of transcripts are poly(A)+, a significant portion of transcripts are either poly(A)- or bimorphic, being found in both the poly(A)+ and poly(A)- populations. Further analyses revealed that many mRNAs may not contain classical long poly(A) tails and such messages are overrepresented in specific functional categories. In addition, we surprisingly found that a few excised introns accumulate in cells and thus constitute a new class of non-polyadenylated long non-coding RNAs. Finally, we have identified a specific subset of poly(A)- histone mRNAs, including two histone H1 variants, that are expressed in undifferentiated hESCs and are rapidly diminished upon differentiation; further, these same histone genes are induced upon reprogramming of fibroblasts to induced pluripotent stem cells.

Conclusions: We offer a rich source of data that allows a deeper exploration of the poly(A)- landscape of the eukaryotic transcriptome. The approach we present here also applies to the analysis of the poly(A)- transcriptomes of other organisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Differentiation
  • Computational Biology / methods*
  • Embryonic Stem Cells / metabolism
  • Eukaryota
  • Gene Expression Regulation
  • Genome*
  • HeLa Cells
  • High-Throughput Nucleotide Sequencing
  • Histones / genetics*
  • Histones / metabolism
  • Humans
  • Introns / genetics*
  • Poly A / genetics
  • Protein Isoforms / genetics*
  • Protein Isoforms / metabolism
  • RNA / genetics*
  • Transcriptome*

Substances

  • Histones
  • Protein Isoforms
  • Poly A
  • RNA