-
Je něco špatně v tomto záznamu ?
The frequency of precocious segregation of sister chromatids in mouse female meiosis I is affected by genetic background
A. Danylevska, K. Kovacovicova, T. Awadova, M. Anger,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 1997-02-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2010-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-02-01 do Před 1 rokem
- MeSH
- aneuploidie MeSH
- chromatidy genetika MeSH
- meióza genetika MeSH
- myši inbrední C3H MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- oocyty cytologie MeSH
- počet buněk MeSH
- polární tělísko metabolismus MeSH
- segregace chromozomů genetika MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Mammalian female gametes frequently suffer from numerical chromosomal aberrations, the main cause of miscarriages and severe developmental defects. The underlying mechanisms responsible for the development of aneuploidy in oocytes are still not completely understood and remain a subject of extensive research. From studies focused on prevalence of aneuploidy in mouse oocytes, it has become obvious that reported rates of aneuploidy are strongly dependent on the method used for chromosome counting. In addition, it seems likely that differences between mouse strains could influence the frequency of aneuploidy as well; however, up till now, such a comparison has not been available. Therefore, in our study, we measured the levels of aneuploidy which has resulted from missegregation in meiosis I, in oocytes of three commonly used mouse strains-CD-1, C3H/HeJ, and C57BL/6. Our results revealed that, although the overall chromosomal numerical aberration rates were similar in all three strains, a different number of oocytes in each strain contained prematurely segregated sister chromatids (PSSC). This indicates that a predisposition for this type of chromosome segregation error in oocyte meiosis I is dependent on genetic background.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15031998
- 003
- CZ-PrNML
- 005
- 20240326132859.0
- 007
- ta
- 008
- 151005s2014 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s10577-014-9428-6 $2 doi
- 035 __
- $a (PubMed)24935618
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Mac Gillavry Danylevska, Anna, $d 1983- $u Veterinary Research Institute, Hudcova 70, 621 00, Brno, Czech Republic. $7 xx0315558
- 245 14
- $a The frequency of precocious segregation of sister chromatids in mouse female meiosis I is affected by genetic background / $c A. Danylevska, K. Kovacovicova, T. Awadova, M. Anger,
- 520 9_
- $a Mammalian female gametes frequently suffer from numerical chromosomal aberrations, the main cause of miscarriages and severe developmental defects. The underlying mechanisms responsible for the development of aneuploidy in oocytes are still not completely understood and remain a subject of extensive research. From studies focused on prevalence of aneuploidy in mouse oocytes, it has become obvious that reported rates of aneuploidy are strongly dependent on the method used for chromosome counting. In addition, it seems likely that differences between mouse strains could influence the frequency of aneuploidy as well; however, up till now, such a comparison has not been available. Therefore, in our study, we measured the levels of aneuploidy which has resulted from missegregation in meiosis I, in oocytes of three commonly used mouse strains-CD-1, C3H/HeJ, and C57BL/6. Our results revealed that, although the overall chromosomal numerical aberration rates were similar in all three strains, a different number of oocytes in each strain contained prematurely segregated sister chromatids (PSSC). This indicates that a predisposition for this type of chromosome segregation error in oocyte meiosis I is dependent on genetic background.
- 650 _2
- $a aneuploidie $7 D000782
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a počet buněk $7 D002452
- 650 _2
- $a chromatidy $x genetika $7 D002842
- 650 _2
- $a segregace chromozomů $x genetika $7 D020090
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a meióza $x genetika $7 D008540
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední C3H $7 D008809
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a oocyty $x cytologie $7 D009865
- 650 _2
- $a polární tělísko $x metabolismus $7 D059705
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kovacovicova, Kristina
- 700 1_
- $a Awadova, Thuraya $7 gn_A_00010457
- 700 1_
- $a Anger, Martin $7 gn_A_00006952
- 773 0_
- $w MED00002161 $t Chromosome research $x 1573-6849 $g Roč. 22, č. 3 (2014), s. 365-73
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24935618 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20151005 $b ABA008
- 991 __
- $a 20240326132856 $b ABA008
- 999 __
- $a ok $b bmc $g 1092874 $s 915124
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 22 $c 3 $d 365-73 $e 20140617 $i 1573-6849 $m Chromosome research $n Chromosome Res $x MED00002161
- LZP __
- $a Pubmed-20151005