Mice with this conditional insertion, upon cre recombinase expression, produce a mutant neurogenin 3 protein in which serine has been replaced by alanine at amino acid positions 183 and 187 (S183A/S187A), eliminating a glycogen synthase kinase 3 beta (GSK3beta) consensus phosphorylation site, impairing its association with FBW7 and stabilizing the protein. The targeting construct was made by insertion of a cDNA encoding the full-length mouse protein with the introduced mutations into the Gateway compatible pROSA26-DV1 plasmid. The final construct contains a splice acceptor followed by a loxP-flanked Pgk-neor with a triple polyadenylation signal (STOP sequence), the modified Neurog3 cDNA, and an enhanced green fluorescent protein (EGFP) cDNA downstream of an internal ribosomal entry site (IRES). Deletion of the Pgk-neor-STOP by cre recombinase results in co-expression of NEUROG3-S183A/S187A and EGFP. (J:194078, J:215154)
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模型ID
品系来源
等位基因类型
突变
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相关疾病
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(129S6/SvEvTac x C57BL/6NCrl)F1
Targeted
Insertion
Dominant
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2

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标签摘要:
hm: 纯合子
ht: 杂合子
cn: 条件基因型
cx: 复合型:涉及多基因组
tg: 转基因
ot: 其他:半合子、不确定...
(F): 雌性
(M): 雄性
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N: 正常表型
(#): 上标括号内为相关疾病数量
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