A case of mosaic deletion of paternally-inherited PLAGL1 and two cases of upd(6)mat add to evidence for PLAGL1 under-expression as a cause of growth restriction

Am J Med Genet A. 2024 Feb;194(2):383-388. doi: 10.1002/ajmg.a.63448. Epub 2023 Oct 18.

Abstract

PLAGL1 is one of a group of imprinted genes, whose altered expression causes imprinting disorders impacting growth, development, metabolism, and behavior. PLAGL1 over-expression causes transient neonatal diabetes mellitus (TNDM type 1) and, based on murine models, under-expression would be expected to cause growth restriction. However, only some reported individuals with upd(6)mat have growth restriction, giving rise to uncertainty about the role of PLAGL1 in human growth. Here we report three individuals investigated for growth restriction, two with upd(6)mat and one with a mosaic deletion of the paternally-inherited allele of PLAGL1. These cases add to evidence of its involvement in pre- and early post-natal human growth.

Keywords: chromomosome 6; genomic imprinting; growth restriction; uniparental disomy; upd(6)mat.

Publication types

  • Case Reports

MeSH terms

  • Animals
  • Cell Cycle Proteins / genetics
  • Genomic Imprinting* / genetics
  • Humans
  • Infant, Newborn
  • Mice
  • Transcription Factors / genetics
  • Tumor Suppressor Proteins / genetics
  • Uniparental Disomy*

Substances

  • PLAGL1 protein, human
  • Transcription Factors
  • Cell Cycle Proteins
  • Tumor Suppressor Proteins