ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

Nucleic Acids Res. 2005 May 11;33(8):2650-60. doi: 10.1093/nar/gki555. Print 2005.

Abstract

Loss of genomic imprinting is involved in a number of developmental abnormalities and cancers. ZAC is an imprinted gene expressed from the paternal allele of chromosome 6q24 within a region known to harbor a tumor suppressor gene for several types of neoplasia. p57(KIP2) (CDKN1C) is a maternally expressed gene located on chromosome 11p15.5 which encodes a cyclin-dependent kinase inhibitor that may also act as a tumor suppressor gene. Mutations in ZAC and p57KIP2 have been implicated in transient neonatal diabetes mellitus (TNDB) and Beckwith-Wiedemann syndrome, respectively. Patients with these diseases share many characteristics. Here we show that mouse Zac1 and p57Kip2 have a strikingly similar expression pattern. ZAC, a sequence-specific DNA-binding protein, binds within the CpG island of LIT1 (KCNQ1OT1), a paternally expressed, anti-sense RNA thought to negatively regulate p57(KIP2) in cis. ZAC induces LIT1 transcription in a methylation-dependent manner. Our data suggest that ZAC may regulate p57(KIP2) through LIT1, forming part of a novel signaling pathway regulating cell growth. Mutations in ZAC may, therefore, contribute to Beckwith-Wiedemann syndrome. Furthermore, we find changes in DNA methylation at the LIT1 putative imprinting control region in two patients with TNDB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Beckwith-Wiedemann Syndrome / genetics*
  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • CpG Islands
  • Cyclin-Dependent Kinase Inhibitor p57
  • DNA Methylation
  • Diabetes Mellitus / genetics
  • Epigenesis, Genetic
  • Gene Expression
  • Gene Silencing
  • Genes, Tumor Suppressor
  • Genetic Predisposition to Disease
  • Genomic Imprinting*
  • Humans
  • Membrane Proteins / genetics*
  • Mice
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Potassium Channels, Voltage-Gated / genetics*
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Transfection
  • Tumor Suppressor Proteins

Substances

  • CDKN1C protein, human
  • Cdkn1c protein, mouse
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p57
  • KCNQ1OT1 long non-coding RNA, human
  • Membrane Proteins
  • Nuclear Proteins
  • PLAGL1 protein, human
  • Plagl1 protein, mouse
  • Potassium Channels, Voltage-Gated
  • Transcription Factors
  • Tumor Suppressor Proteins