Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Analysis of transactivation capability and conformation of p53 temperature-dependent mutants and their reactivation by amifostine in yeast

D Grochova, J Vankova, J Damborsky, B Ravcukova, J Smarda, B Vojtesek, J Smardova

. 2008 ; 27 (9) : 1243-1252.

Language English Country Great Britain

Grant support
NR8068 MZ0 CEP Register

Digital library NLK
Full text - Část
Source

E-resources

NLK ProQuest Central from 2000-01-01 to 1 year ago
Open Access Digital Library from 1997-01-01
Medline Complete (EBSCOhost) from 1997-01-09 to 2015-11-26
Health & Medicine (ProQuest) from 2000-01-01 to 1 year ago
Public Health Database (ProQuest) from 2000-01-01 to 1 year ago

The p53 gene is often mutated during cancer development. Frequency and functional consequences of these mutations vary in different tumor types. We analysed conformation and temperature dependency of 23 partially inactivating temperature-dependent (td) p53 mutants derived from various human tumors in yeast. We found considerable differences in transactivation capabilities and discriminative character of various p53 mutants. No correlations in transactivation rates and conformations of the td p53 proteins were detected. Amifostine-induced p53 reactivation occurred only in 13 of 23 td mutants, and this effect was temperature dependent and responsive element specific. The most of the p53 mutations (10/13) reactivated by amifostine were located in the part of the p53 gene coding for hydrophobic beta-sandwich structure of the DNA-binding domain.

000      
00000naa 2200000 a 4500
001      
bmc10026412
003      
CZ-PrNML
005      
20130814101910.0
008      
101018s2008 xxk e eng||
009      
AR
040    __
$a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Nikulenkov Grochová, Diana. $7 mub20181016842
245    10
$a Analysis of transactivation capability and conformation of p53 temperature-dependent mutants and their reactivation by amifostine in yeast / $c D Grochova, J Vankova, J Damborsky, B Ravcukova, J Smarda, B Vojtesek, J Smardova
314    __
$a Department of Pathology, University Hospital, Brno, Czech Republic.
520    9_
$a The p53 gene is often mutated during cancer development. Frequency and functional consequences of these mutations vary in different tumor types. We analysed conformation and temperature dependency of 23 partially inactivating temperature-dependent (td) p53 mutants derived from various human tumors in yeast. We found considerable differences in transactivation capabilities and discriminative character of various p53 mutants. No correlations in transactivation rates and conformations of the td p53 proteins were detected. Amifostine-induced p53 reactivation occurred only in 13 of 23 td mutants, and this effect was temperature dependent and responsive element specific. The most of the p53 mutations (10/13) reactivated by amifostine were located in the part of the p53 gene coding for hydrophobic beta-sandwich structure of the DNA-binding domain.
650    _2
$a amifostin $x farmakologie $7 D004999
650    _2
$a substituce aminokyselin $x genetika $7 D019943
650    _2
$a lidé $7 D006801
650    _2
$a konformace proteinů $x účinky léků $7 D011487
650    _2
$a radioprotektivní látky $x farmakologie $7 D011837
650    _2
$a Saccharomyces cerevisiae - proteiny $x genetika $x účinky léků $7 D029701
650    _2
$a teplota $7 D013696
650    _2
$a aktivace transkripce $x genetika $x účinky léků $7 D015533
650    _2
$a aktivace transkripce $x genetika $7 D015533
650    _2
$a nádorový supresorový protein p53 $x biosyntéza $x genetika $x chemie $7 D016159
650    _2
$a financování organizované $7 D005381
700    1_
$a Vaňková, J. $7 _AN038365
700    1_
$a Damborský, Jiří, $d 1969- $7 mzk2006348900
700    1_
$a Ravčuková, Barbora $7 xx0105242
700    1_
$a Šmarda, Jan, $d 1961- $7 mzk2006343362
700    1_
$a Vojtěšek, Bořivoj, $d 1960- $7 xx0001694
700    1_
$a Šmardová, Jana, $d 1961- $7 mzk2005304278
773    0_
$w MED00003600 $t Oncogene $g Roč. 27, č. 9 (2008), s. 1243-1252 $x 0950-9232
910    __
$a ABA008 $b x $y 7
990    __
$a 20110112144541 $b ABA008
991    __
$a 20130814102419 $b ABA008
999    __
$a ok $b bmc $g 801517 $s 666267
BAS    __
$a 3
BMC    __
$a 2008 $b 27 $c 9 $d 1243-1252 $m Oncogene $n Oncogene $x MED00003600
GRA    __
$a NR8068 $p MZ0
LZP    __
$a 2010-B/mk

Find record