Cloning and functional analysis of human p51, which structurally and functionally resembles p53 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1998-07

AUTHORS

Motonobu Osada, Mai Ohba, Chikashi Kawahara, Chikashi Ishioka, Ryunosuke Kanamaru, Iyoko Katoh, Yoji Ikawa, Yoshinori Nimura, Akira Nakagawara, Masuo Obinata, Shuntaro Ikawa

ABSTRACT

The p53 tumor suppressor gene, which is induced by DNA damage and/or stress stimuli, causes cells to undergo G1-arrest or apoptotic death; thus it plays an essential role in human carcinogenesis. We have searched for p53-related genes by using degenerate PCR, and have identified two cDNA fragments similar to but distinct from p53: one previously reported, p73, and the other new. We cloned two major splicing variants of the latter gene and named these p51A and p51B (a human homologue of rat Ket). The p51A gene encodes a 448-amino-acid protein with a molecular weight of 50.9 kDa; and p51B, a 641-amino-acid protein with a molecular weight of 71.9 kDa. In contrast with the ubiquitous expression of p53, expression of p51 mRNA was found in a limited number of tissues, including skeletal muscle, placenta, mammary gland, prostate, trachea, thymus, salivary gland, uterus, heart and lung. In p53-deficient cells, p51A induced growth-suppression and apoptosis, and upregulated p21waf-1 through p53 regulatory elements. Mutations in p51 were found in some human epidermal tumors. More... »

PAGES

839-843

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/nm0798-839

DOI

http://dx.doi.org/10.1038/nm0798-839

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1038067182

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/9662378


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