Abnormal RNA processing and altered expression of serin-rich proteins in minimal-change nephrotic syndrome

Pediatr Res. 2005 Jan;57(1):133-7. doi: 10.1203/01.PDR.0000148013.53429.5B. Epub 2004 Nov 5.

Abstract

Mechanisms underlying the pathophysiology of minimal-change nephrotic syndrome (MCNS), the most frequent glomerular disease in children, remain elusive, but recent findings argue for a T cell dysfunction. Starting from a differential cDNA library from T cells of a patient under relapse and remission, we identified 16 transcripts specific for MCNS. All of these transcripts that were selectively up-regulated during the relapse phase of the disease were generated by alternative splicing of known genes. This abnormal RNA expression was associated with a down-regulation of serin-rich protein 75 and serin-rich protein 40, two proteins involved in mRNA splicing. Taken together, these data suggest that T cell dysfunction in MCNS is associated with abnormal mRNA splicing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Child
  • Cohort Studies
  • DNA Primers / chemistry
  • DNA, Complementary / metabolism
  • Down-Regulation
  • Gene Library
  • Humans
  • Immunohistochemistry
  • Nephrotic Syndrome / genetics
  • Nephrotic Syndrome / metabolism*
  • Phosphorylation
  • RNA / metabolism
  • RNA Processing, Post-Transcriptional
  • RNA, Messenger / metabolism
  • Recurrence
  • Remission Induction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Serine / metabolism*
  • T-Lymphocytes / cytology
  • Up-Regulation

Substances

  • DNA Primers
  • DNA, Complementary
  • RNA, Messenger
  • Serine
  • RNA