Identification of two new exons and multiple transcription start points in the 5′-untranslated region of the human cathepsin-B-encoding gene

Isabelle M. Berquin, Lequn Cao, Dunne Fong, Bonnie F. Sloane

Research output: Contribution to journalArticlepeer-review

64 Scopus citations

Abstract

Transcripts for cysteine protease cathepsin B (CTSB) were found to be highly variable in the 5′-UTR (untranslated region). In cDNA clones from a human gastric adenocarcinoma cDNA library, we have identified two new exons (designated 2a and 2b) between exons 2 and 3 in the 5′-UTR of the gene. All of the exons of the 5′-UTR could be alternatively spliced to produce several transcript species. In addition, transcription was initiated from more than one promoter region. Using RT-PCR (reverse transcription-polymerase chain reaction) and primer extension assays, CTSB mRNA species were found to differ among tissues and between a glioblastoma sample and a cell line derived from it. Exons 2a and 2b were detected more frequently in tumor samples than in matched normal samples. Thus, factors related to the cell differentiation and environment seem likely to determine the types of transcripts that are expressed which in turn could influence the overall steady-state level of CTSB mRNAs and their rate of translation. Interestingly, at least three upstream translation initiation codons were observed and could constitute a means of controlling translation initiation.

Original languageEnglish (US)
Pages (from-to)143-149
Number of pages7
JournalGene
Volume159
Issue number2
DOIs
StatePublished - 1995

All Science Journal Classification (ASJC) codes

  • Genetics

Keywords

  • Cysteine protease
  • RNA splicing
  • glioblastoma
  • post-transcriptional regulation
  • promoter
  • tumor

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