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Characterization of the murine CD30 ligand (CD153) gene: gene structure and expression

L C Goldie-Cregan1, E J Croager, L J Abraham

  • 1The University of Western Australia, Crawley.

Tissue Antigens
|October 24, 2002
PubMed

Insights

This study details the murine CD153 gene structure, revealing its four exons and promoter region. We identified multiple transcriptional start and polyadenylation sites, influencing CD153 transcript length.

Area of Science:

  • Immunology
  • Molecular Biology
  • Genomics

Background:

  • CD153, also known as CD30 ligand, is a type II transmembrane glycoprotein within the TNF superfamily.
  • It is primarily expressed on activated T cells, B cells, and monocytes.

Purpose of the Study:

  • To elucidate the genomic structure of the murine CD153 gene.
  • To identify regulatory elements and transcriptional start sites of murine CD153.

Main Methods:

  • Genomic sequence analysis of the murine CD153 gene.
  • Sequence analysis of the promoter and 5' flanking region.
  • 5' RACE (Rapid Amplification of cDNA Ends) analysis on LPS-stimulated macrophage cDNA.

Main Results:

  • The murine CD153 gene comprises four exons spanning approximately 26 kb.
  • Analysis revealed a TATA box and putative lymphoid-specific transcription factor binding motifs in the promoter region.
  • Multiple transcriptional start sites and polyadenylation sites were identified, suggesting transcript length variation from 26 kb to 28 kb.

Conclusions:

  • The murine CD153 gene structure and regulatory elements provide insight into its expression control.
  • The identified transcriptional and polyadenylation sites contribute to the heterogeneity of primary CD153 transcripts.

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