KŘÍŽ, Vítězslav, Jaroslav MAREŠ, Parri WENTZEL, Nina FUNA, Gabriela ČALOUNOVÁ, Xiao-Qun ZHANG, Karin FORSBERG-NILSSON, Maud FORSBERG a Michael WELSH. Shb null allele is inherited with a transmission ratio distortion and causes reduced viability in utero. Developmental dynamics. United States: Wiley-Liss, 2007, roč. 236, č. 9, s. 2485-2492. ISSN 1058-8388. Dostupné z: https://dx.doi.org/10.1002/dvdy.21257.
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Základní údaje
Originální název Shb null allele is inherited with a transmission ratio distortion and causes reduced viability in utero.
Název česky Shb null allele is inherited with a transmission ratio distortion and causes reduced viability in utero.
Autoři KŘÍŽ, Vítězslav (203 Česká republika, garant, domácí), Jaroslav MAREŠ (203 Česká republika), Parri WENTZEL (752 Švédsko), Nina FUNA (752 Švédsko), Gabriela ČALOUNOVÁ (203 Česká republika), Xiao-Qun ZHANG (156 Čína), Karin FORSBERG-NILSSON (752 Švédsko), Maud FORSBERG (752 Švédsko) a Michael WELSH (840 Spojené státy).
Vydání Developmental dynamics, United States, Wiley-Liss, 2007, 1058-8388.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor Genetika a molekulární biologie
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 3.084
Kód RIV RIV/00216224:14310/07:00050891
Organizační jednotka Přírodovědecká fakulta
Doi http://dx.doi.org/10.1002/dvdy.21257
UT WoS 000249539700012
Klíčová slova anglicky SHB; knockout; ovulation; malformations; viability in utero; transmission ratio distortion
Štítky AKR, knockout, malformations, ovulation, rivok, SHB, transmission ratio distortion, viability in utero
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Ing. Andrea Mikešková, učo 137293. Změněno: 13. 4. 2012 12:07.
Anotace
SHB is an Src homology 2 domain-containing adapter protein that has been found to be involved in numerous cellular responses. We have generated an Shb knockout mouse. No Shb-/- pups or embryos were obtained on the C57Bl6 background, indicating an early defect as a consequence of Shb- gene inactivation on this genetic background. Breeding heterozygotes for Shb gene inactivation (Shb+/-) on a mixed genetic background (FVB/C57Bl6/129Sv) reveals a distorted transmission ratio of the null allele with reduced numbers of Shb+/+ and Shb-/- animals, but increased number of Shb+/- animals. The Shb- allele is associated with various forms of malformations, explaining the relative reduction in the number of Shb-/- offspring. Shb-/- animals that were born were viable, fertile, and showed no obvious defects. However, Shb+/- female mice ovulated preferentially Shb- oocytes explaining the reduced frequency of Shb+/+ mice. Our study suggests a role of SHB during reproduction and development.
Anotace česky
SHB is an Src homology 2 domain-containing adapter protein that has been found to be involved in numerous cellular responses. We have generated an Shb knockout mouse. No Shb-/- pups or embryos were obtained on the C57Bl6 background, indicating an early defect as a consequence of Shb- gene inactivation on this genetic background. Breeding heterozygotes for Shb gene inactivation (Shb+/-) on a mixed genetic background (FVB/C57Bl6/129Sv) reveals a distorted transmission ratio of the null allele with reduced numbers of Shb+/+ and Shb-/- animals, but increased number of Shb+/- animals. The Shb- allele is associated with various forms of malformations, explaining the relative reduction in the number of Shb-/- offspring. Shb-/- animals that were born were viable, fertile, and showed no obvious defects. However, Shb+/- female mice ovulated preferentially Shb- oocytes explaining the reduced frequency of Shb+/+ mice. Our study suggests a role of SHB during reproduction and development.
VytisknoutZobrazeno: 13. 5. 2024 17:55