-
Something wrong with this record ?
CDKA and CDKB kinases from Chlamydomonas reinhardtii are able to complement cdc28 temperature-sensitive mutants of Saccharomyces cerevisiae
Čížková M., Pichová A., Vítová M., Hlavová M., Hendrychová J., Umysová D., Gálová E., Sevcovicová A., Zachleder V., Umen J.G., Bisová K.
Language English Country Austria
NLK
ProQuest Central
from 2003-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2007-01-01 to 1 year ago
Nursing & Allied Health Database (ProQuest)
from 2003-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 2003-01-01 to 1 year ago
Psychology Database (ProQuest)
from 2003-01-01 to 1 year ago
- MeSH
- Chlamydomonas reinhardtii enzymology MeSH
- Cyclin-Dependent Kinases chemistry metabolism MeSH
- Financing, Organized MeSH
- Molecular Sequence Data MeSH
- Mutation genetics MeSH
- CDC28 Protein Kinase, S cerevisiae metabolism MeSH
- Saccharomyces cerevisiae cytology enzymology MeSH
- Amino Acid Sequence MeSH
- Sequence Alignment MeSH
- Temperature MeSH
- Genetic Complementation Test MeSH
- Transformation, Genetic MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
Cyclin-dependent kinases (CDK) play a key role in coordinating cell division in all eukaryotes. We investigated the capability of cyclin-dependent kinases CDKA and CDKB from the green alga Chlamydomonas reinhardtii to complement a Saccharomyces cerevisiae cdc28 temperature-sensitive mutant. The full-length coding regions of algal CDKA and CDKB cDNA were amplified by RT-PCR and cloned into the yeast expression vector pYES-DEST52, yielding pYD52-CDKA and pYD52-CDKB. The S. cerevisiae cdc28-1N strain transformed with these constructs exhibited growth at 36 degrees C in inducing (galactose) medium, but not in repressing (glucose) medium. Microscopic observation showed that the complemented cells had the irregular cylindrical shape typical for G2 phase-arrested cells when grown on glucose at 36 degrees C, but appeared as normal budded cells when grown on galactose at 36 degrees C. Sequence analysis and complementation tests proved that both CDKA and CDKB are functional CDC28/cdc2 homologs in C. reinhardtii. The complementation of the mitotic phenotype of the S. cerevisiae cdc28-1N mutant suggests a mitotic role for both of the kinases.
- 000
- 00000naa 2200000 a 4500
- 001
- bmc11004061
- 003
- CZ-PrNML
- 005
- 20120121003210.0
- 008
- 110303s2008 au e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a au
- 100 1_
- $a Čížková, Mária, $d 1980- $7 xx0137526
- 245 10
- $a CDKA and CDKB kinases from Chlamydomonas reinhardtii are able to complement cdc28 temperature-sensitive mutants of Saccharomyces cerevisiae / $c Čížková M., Pichová A., Vítová M., Hlavová M., Hendrychová J., Umysová D., Gálová E., Sevcovicová A., Zachleder V., Umen J.G., Bisová K.
- 314 __
- $a Laboratory of Cell Cycles of Algae, Institute of Microbiology, Academy of Sciences of the Czech Republic, Trebon, Czech Republic
- 520 9_
- $a Cyclin-dependent kinases (CDK) play a key role in coordinating cell division in all eukaryotes. We investigated the capability of cyclin-dependent kinases CDKA and CDKB from the green alga Chlamydomonas reinhardtii to complement a Saccharomyces cerevisiae cdc28 temperature-sensitive mutant. The full-length coding regions of algal CDKA and CDKB cDNA were amplified by RT-PCR and cloned into the yeast expression vector pYES-DEST52, yielding pYD52-CDKA and pYD52-CDKB. The S. cerevisiae cdc28-1N strain transformed with these constructs exhibited growth at 36 degrees C in inducing (galactose) medium, but not in repressing (glucose) medium. Microscopic observation showed that the complemented cells had the irregular cylindrical shape typical for G2 phase-arrested cells when grown on glucose at 36 degrees C, but appeared as normal budded cells when grown on galactose at 36 degrees C. Sequence analysis and complementation tests proved that both CDKA and CDKB are functional CDC28/cdc2 homologs in C. reinhardtii. The complementation of the mitotic phenotype of the S. cerevisiae cdc28-1N mutant suggests a mitotic role for both of the kinases.
- 650 _2
- $a financování organizované $7 D005381
- 650 _2
- $a sekvence aminokyselin $7 D000595
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a proteinkinasa CDC28, S cerevisiae $x metabolismus $7 D017489
- 650 _2
- $a Chlamydomonas reinhardtii $x enzymologie $7 D016825
- 650 _2
- $a cyklin-dependentní kinasy $x chemie $x metabolismus $7 D018844
- 650 _2
- $a testy genetické komplementace $7 D005816
- 650 _2
- $a molekulární sekvence - údaje $7 D008969
- 650 _2
- $a mutace $x genetika $7 D009154
- 650 _2
- $a Saccharomyces cerevisiae $x cytologie $x enzymologie $7 D012441
- 650 _2
- $a sekvenční seřazení $7 D016415
- 650 _2
- $a teplota $7 D013696
- 650 _2
- $a transformace genetická $7 D014170
- 700 1_
- $a Pichová, Alena $7 xx0102259
- 700 1_
- $a Vítová, Milada, $d 1971- $7 xx0031789
- 700 1_
- $a Hlavová, Monika $7 xx0126312
- 700 1_
- $a Hendrychová, Jana. $7 xx0040483
- 700 1_
- $a Umysová, Dáša $7 xx0122665
- 700 1_
- $a Gálová, Eliška. $7 _AN059837
- 700 1_
- $a Ševčovičová, Andrea $7 xx0105041
- 700 1_
- $a Zachleder, Vilém, $d 1944- $7 xx0040499
- 700 1_
- $a Umen, J. G.
- 700 1_
- $a Bišová, Kateřina $7 xx0137525
- 773 0_
- $w MED00014220 $t Protoplasma $g Roč. 232, č. 3-4 (2008), s. 183-191 $x 0033-183X
- 910 __
- $a ABA008 $b x $y 1
- 990 __
- $a 20110303105241 $b ABA008
- 991 __
- $a 20120121003203 $b ABA008
- 999 __
- $a ok $b bmc $g 831401 $s 696089
- BAS __
- $a 3
- BMC __
- $a 2008 $b 232 $c 3-4 $d 183-191 $m Protoplasma $x MED00014220
- LZP __
- $a 2011-3B/ipme