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Complex functional redundancy of Tbx2 and Tbx3 in mouse limb development.
Lopatka, Alika; Moon, Anne M.
Afiliação
  • Lopatka A; Department of Molecular and Functional Genomics, Weis Center for Research, Geisinger Clinic, Danville, Pennsylvania, USA.
  • Moon AM; Department of Molecular and Functional Genomics, Weis Center for Research, Geisinger Clinic, Danville, Pennsylvania, USA.
Dev Dyn ; 251(9): 1613-1627, 2022 09.
Article em En | MEDLINE | ID: mdl-35506352
The limb phenotypes of Tbx2 and Tbx3 mutants are distinct: loss of Tbx2 results in isolated duplication of digit 4 in the hindlimb while loss of Tbx3 results in anterior polydactyly and posterior oligodactly in the forelimb. In the face of such disparate phenotypes, we sought to determine whether Tbx2 and Tbx3 have functional redundancy during development of the mouse limb. We found that sequential loss of alleles generates defects that are not simply additive of those observed in single mutants and that multiple structures in both the forelimb and hindlimb display compound sensitivity to decreased gene dosage.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas com Domínio T / Extremidades Limite: Animals Idioma: En Revista: Dev Dyn Assunto da revista: ANATOMIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas com Domínio T / Extremidades Limite: Animals Idioma: En Revista: Dev Dyn Assunto da revista: ANATOMIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos