Literature DB >> 10331945

Guinea pig p53 mRNA: identification of new elements in coding and untranslated regions and their functional and evolutionary implications.

A M D'erchia1, G Pesole, A Tullo, C Saccone, E Sbisà.   

Abstract

We report the sequence of the guinea pig p53 cDNA. The comparative analysis of the coding and noncoding regions of p53 cDNAs of all available complete vertebrate sequences has allowed us to single out new conserved signals possibly involved in p53 functional activity. We have focused our attention on the most variable region of the protein, the proline (P)-rich domain, suggested to play a fundamental role in antiproliferative pathways. In this domain we have identified the PXXXXP repeated motif and singled out a common consensus sequence that can be considered a signature for mammalian p53: PXXXXPX{0,4}PX{0,9}PA(T,P,I,)(S,P)WPL. We have demonstrated the significance of the PXXXXP motif in SH3-binding protein and suggested its structure to be a loop. Also, the 5' and 3' untranslated regions (UTRs) of the guinea pig were sequenced, and this study represents the first detailed structural analysis of the UTRs of the p53 mRNAs available in literature. The 5' UTR of guinea pig (233 nt) can be folded into a stable secondary structure resembling that predicted in mouse. The 3' UTR of guinea pig is 771 nt long and shows higher similarity with human than with rodent sequences, having a region of about 350 nt that is deleted in rat and mouse. In the 3' UTR we have identified the presence of a mammalian-wide interspersed repeat sequence and of a cytoplasmic polyadenylation element, which could be involved in translational activation by promoting polyadenylation of mRNA, providing information about a possible mechanism of regulation of p53 expression mediated by the 3' UTR of the mRNA. The observations presented here could open new avenues to targeted mutations and experimental approaches useful in investigating new regulation mechanisms of p53 translation, activity, and stability. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10331945     DOI: 10.1006/geno.1999.5794

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  TP53 codon 72 polymorphism in 12 populations of insular Southeast Asia and Oceania.

Authors:  Taeko Kashima; Kumiko Makino; Augustinua Soemantri; Takafumi Ishida
Journal:  J Hum Genet       Date:  2007-07-03       Impact factor: 3.172

2.  Mouse mutants reveal that putative protein interaction sites in the p53 proline-rich domain are dispensable for tumor suppression.

Authors:  Franck Toledo; Crystal J Lee; Kurt A Krummel; Luo-Wei Rodewald; Chung-Wen Liu; Geoffrey M Wahl
Journal:  Mol Cell Biol       Date:  2006-12-11       Impact factor: 4.272

3.  Molecular characterization of p53 mutations in primary and secondary liver tumors: diagnostic and therapeutic perspectives.

Authors:  Apollonia Tullo; Elisabetta Sbisà
Journal:  Mol Biotechnol       Date:  2002-07       Impact factor: 2.695

4.  CPEB4 Inhibit Cell Proliferation via Upregulating p21 mRNA Stability in Renal Cell Carcinoma.

Authors:  Jiehui Di; Hui Wang; Zhongjun Zhao; Guang Zhao; Xiaobing Qin; Zhengxiang Han; Yong Liu
Journal:  Front Cell Dev Biol       Date:  2021-12-16

5.  An ultrasensitive photoelectrochemical nucleic acid biosensor.

Authors:  Zhiqiang Gao; Natalia C Tansil
Journal:  Nucleic Acids Res       Date:  2005-08-01       Impact factor: 16.971

Review 6.  Translational Control in p53 Expression: The Role of 5'-Terminal Region of p53 mRNA.

Authors:  Agata Swiatkowska; Mariola Dutkiewicz; Paulina Zydowicz-Machtel; Joanna Szpotkowska; Damian M Janecki; Jerzy Ciesiołka
Journal:  Int J Mol Sci       Date:  2019-10-29       Impact factor: 5.923

  6 in total

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