Identification of two novel isoforms of mouse NUR77 lacking N-terminal domains

Sayeed Ur Rehman1,2, Tarique Sarwar1,2, Mohammed Amir Husain1,2

  • 1Department of Biochemistry, Faculty of Life Sciences, A.M. University, Aligarh, Uttar Pradesh, India.

IUBMB Life
|January 24, 2017
PubMed

Insights

Researchers discovered two new, smaller Nur77 protein variants in mice, encoded by novel gene transcripts. These variants, with altered domains, are primarily located outside the nucleus, offering new research avenues for this transcription factor.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Nur77, a nuclear receptor superfamily member, functions as a transcription factor regulating gene expression.
  • Subcellular localization of Nur77 is critical for cell survival and death pathways.

Purpose of the Study:

  • To identify and characterize novel alternatively spliced transcripts of the Nur77 gene in mice.
  • To investigate the functional implications of these new Nur77 variants.

Main Methods:

  • Bioinformatic analysis to predict and analyze novel transcripts and their promoter regions.
  • Experimental validation using Western blot analysis to confirm protein variant expression.
  • In silico analysis of protein isoforms using bioinformatics tools.

Main Results:

  • Two novel alternatively spliced Nur77 transcripts were identified in mice, with unique upstream first exons.
  • These new transcripts express smaller NUR77 protein isoforms lacking key functional domains (transactivation and part of DNA binding).
  • Western blot confirmed the presence of these smaller variants, predicted to localize mainly outside the nucleus.

Conclusions:

  • The study reveals novel, smaller Nur77 protein isoforms resulting from alternative splicing.
  • These findings expand the understanding of Nur77's molecular diversity and subcellular localization.
  • This research opens new avenues for investigating Nur77's role in cellular processes.