Cloning and functional analysis of human p51 , which structurally and functionally resembles p53
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 carcinogenesis1,2. We have searched for p53 -related genes by using degenerate PCR, and have identified two cDNA fragmen...
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Veröffentlicht in: | Nature medicine 1998-07, Vol.4 (7), p.839-843 |
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Sprache: | eng |
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Zusammenfassung: | 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 carcinogenesis1,2. 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
(refs. 3,4), 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
p5I
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 up-regulated p21waf-1 through p53 regulatory elements. Mutations in
p51
were found in some human epidermal tumors. |
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ISSN: | 1078-8956 1546-170X |
DOI: | 10.1038/nm0798-839 |