• Je něco špatně v tomto záznamu ?

Protein modification in the post-mating spermatophore of the signal crayfish Pacifastacus leniusculus: insight into the tyrosine phosphorylation in a non-motile spermatozoon

H. Niksirat, M. Vancová, L. Andersson, P. James, A. Kouba, P. Kozák,

. 2016 ; 172 (-) : 123-30. [pub] 20160715

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc17013608

After mating, spermatophores of signal crayfish are stored on the body of the female for a period before fertilization. This study compared the post-mating protein profile and pattern of protein tyrosine phosphorylation of the signal crayfish spermatophore to that of the freshly ejaculated spermatophore and found substantial differences. Two major bands of tyrosine-phosphorylated proteins of molecular weights 10 and 50kDa were observed in the freshly ejaculated spermatophore of the signal crayfish. While the tyrosine-phosphorylated protein band with molecular weight 10kDa was formed by protein(s) of similar pH, the band with molecular weight of 50kDa consisted of proteins of varying pH. In the post-mating spermatophore, the band with molecular weight of 50kDa was not detected, and an increase in the level of protein tyrosine phosphorylation was observed in the 10kDa band. The microtubular radial arms of the spermatozoon showed a positive reaction to an anti-tyrosine antibody conjugated with gold particles in both the freshly ejaculated and post-mating spermatophores. In conclusion, the male gamete of the signal crayfish undergoes molecular modification during post-mating storage on the body of the female including changes in the level of protein expression and protein tyrosine phosphorylation. Structural similarity of the radial arms in the crayfish immotile spermatozoon with flagellum, which is the main site of protein tyrosine phosphorylation in the mammalian motile spermatozoa, raises questions regarding evolution and function of such organelles across the animal kingdom that must be addressed in the future studies.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17013608
003      
CZ-PrNML
005      
20170425100603.0
007      
ta
008      
170413s2016 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.anireprosci.2016.07.009 $2 doi
035    __
$a (PubMed)27481552
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Niksirat, Hamid $u University of South Bohemia in České Budějovice, Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Research Institute of Fish Culture and Hydrobiology, Zátiší 728/II, 38925 Vodňany, Czech Republic. Electronic address: niksirat@frov.jcu.cz.
245    10
$a Protein modification in the post-mating spermatophore of the signal crayfish Pacifastacus leniusculus: insight into the tyrosine phosphorylation in a non-motile spermatozoon / $c H. Niksirat, M. Vancová, L. Andersson, P. James, A. Kouba, P. Kozák,
520    9_
$a After mating, spermatophores of signal crayfish are stored on the body of the female for a period before fertilization. This study compared the post-mating protein profile and pattern of protein tyrosine phosphorylation of the signal crayfish spermatophore to that of the freshly ejaculated spermatophore and found substantial differences. Two major bands of tyrosine-phosphorylated proteins of molecular weights 10 and 50kDa were observed in the freshly ejaculated spermatophore of the signal crayfish. While the tyrosine-phosphorylated protein band with molecular weight 10kDa was formed by protein(s) of similar pH, the band with molecular weight of 50kDa consisted of proteins of varying pH. In the post-mating spermatophore, the band with molecular weight of 50kDa was not detected, and an increase in the level of protein tyrosine phosphorylation was observed in the 10kDa band. The microtubular radial arms of the spermatozoon showed a positive reaction to an anti-tyrosine antibody conjugated with gold particles in both the freshly ejaculated and post-mating spermatophores. In conclusion, the male gamete of the signal crayfish undergoes molecular modification during post-mating storage on the body of the female including changes in the level of protein expression and protein tyrosine phosphorylation. Structural similarity of the radial arms in the crayfish immotile spermatozoon with flagellum, which is the main site of protein tyrosine phosphorylation in the mammalian motile spermatozoa, raises questions regarding evolution and function of such organelles across the animal kingdom that must be addressed in the future studies.
650    _2
$a zvířata $7 D000818
650    _2
$a severní raci $x fyziologie $7 D003400
650    _2
$a kopulace $7 D003307
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a fosforylace $x fyziologie $7 D010766
650    _2
$a proteiny $x genetika $x metabolismus $7 D011506
650    _2
$a motilita spermií $x fyziologie $7 D013081
650    _2
$a spermatogonie $x fyziologie $7 D013093
650    _2
$a spermie $x fyziologie $7 D013094
650    _2
$a tyrosin $x metabolismus $7 D014443
655    _2
$a časopisecké články $7 D016428
700    1_
$a Vancová, Marie $u Institute of Parasitology, Biology Centre of the ASCR and Faculty of Science, University of South Bohemia in České Budějovice, Branišovská 31, České Budějovice 37005, Czech Republic.
700    1_
$a Andersson, Liselotte $u Department of Immunotechnology, Hus 406, Medicon Village, Lund University, 22381, Lund, Sweden. $7 gn_A_00006208
700    1_
$a James, Peter $u Department of Immunotechnology, Hus 406, Medicon Village, Lund University, 22381, Lund, Sweden.
700    1_
$a Kouba, Antonín $u University of South Bohemia in České Budějovice, Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Research Institute of Fish Culture and Hydrobiology, Zátiší 728/II, 38925 Vodňany, Czech Republic.
700    1_
$a Kozák, Pavel $u University of South Bohemia in České Budějovice, Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Research Institute of Fish Culture and Hydrobiology, Zátiší 728/II, 38925 Vodňany, Czech Republic.
773    0_
$w MED00006160 $t Animal reproduction science $x 1873-2232 $g Roč. 172, č. - (2016), s. 123-30
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27481552 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20170413 $b ABA008
991    __
$a 20170425100921 $b ABA008
999    __
$a ok $b bmc $g 1200073 $s 974386
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2016 $b 172 $c - $d 123-30 $e 20160715 $i 1873-2232 $m Animal reproduction science $n Anim Reprod Sci $x MED00006160
LZP    __
$a Pubmed-20170413

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...