Transcription and polyadenylation in a short human intergenic region

Nucleic Acids Res. 1997 Jun 15;25(12):2326-36. doi: 10.1093/nar/25.12.2326.

Abstract

The poly(A) signal of the human Lamin B2 gene was previously shown to lie 600 bp upstream of the cap site of a gene of unknown function (ppv 1). However, using RNase protection analysis, we show that ppv 1 has two clusters of multiple initiation sites, so that the 5"cap site lies only approximately 280 nt downstream of the Lamin B2 poly(A) signal. We analysed nascent transcription across this unusually short intergenic region using nuclear run-on analysis of both the endogenous locus and of transiently transfected hybrid constructs. Surprisingly, transcription of the Lamin B2 gene does not appear to terminate prior to any of the mapped ppv 1 start sites, although pausing of the elongating polymerase complexes is observed downstream of the Lamin B2 poly(A) signal. We suggest that this pausing may be sufficient to protect the downstream gene from transcriptional interference. Finally, we have also investigated the sequences required for efficient recognition of the Lamin B2 poly(A) signal. We show that sequences upstream of the AAUAAA element are required for full activity, which is an unusual feature of mammalian poly(A) signals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cell Nucleus / metabolism
  • Chromosome Mapping
  • Chromosomes, Human, Pair 19*
  • HeLa Cells
  • Humans
  • Introns*
  • Lamin Type B*
  • Lamins
  • Nuclear Proteins / biosynthesis*
  • Nuclear Proteins / genetics*
  • Poly A / metabolism*
  • RNA Caps
  • Recombinant Proteins / biosynthesis
  • Regulatory Sequences, Nucleic Acid
  • Restriction Mapping
  • Transcription, Genetic*
  • Transfection

Substances

  • Lamin Type B
  • Lamins
  • Nuclear Proteins
  • RNA Caps
  • Recombinant Proteins
  • Poly A