Open AccessStructure of the promoter and complete sequence of the gene coding for the rabbit translationally controlled tumor protein (TCTP) P23
Author(s) -
Thiele Holger,
Berger Mario,
Lenzner Claudia,
Kühn Hartmut,
Thiele BerndJoachim
Publication year - 1998
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1046/j.1432-1327.1998.2570062.x
Subject(s) - tata box , biology , microbiology and biotechnology , gene , polyadenylation , promoter , pseudogene , exon , coding region , untranslated region , sox4 , intron , genetics , gene expression , messenger rna , genome
We have isolated genomic recombinants containing the complete gene coding for the rabbit translationally controlled tumor protein (TCTP), also known as histamine‐releasing factor (HRF) P23. The gene is organized into five introns and six exons and its total length amounts to 3819 nucleotides. All intron/exon boundaries are in accordance with the GT/AG rule. Transcription of the gene generates two mRNAs of 843 and 1163 nucleotides differing in the length of their 3′‐untranslated regions. They are formed by alternative polyadenylation. The transcription initiation site has been determined by comparison of sequences of the gene and several processed TCTP pseudogenes. The full‐length 5′‐untranslated region comprises 116 nucleotides and starts with an oligopyrimidine tract important for translational regulation. Additionally 1.2 kb of the 5′‐flanking promoter region has been sequenced. The promoter contains a TATA box at −30 and potential binding sites for transcription factors such as stimulating protein 1 (Sp1), nuclear factor 1 (NF1), activator protein 1 (AP1), c‐Ets1, cAMP‐response element (CP2), myeloid‐specific zinc finger protein 1 (MZF1) and others. For functional analysis 5′‐flanking sequences up to −918 were fused to the chloramphenicol acetyltransferase (CAT) gene and tested using a rabbit aortic smooth‐muscle cell line by cell transfection and CAT assays. The results confirm that the analyzed gene is the actively transcribed TCTP gene.