Consequences of Cre-mediated deletion of Ciz1 exon 5 in mice.

Consequences of Cre-mediated deletion of Ciz1 exon 5 in mice.
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DOI:
10.1002/1873-3468.13221
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发表时间:
2018-09
期刊:
影响因子:
3.5
通讯作者:
LeDoux MS
LeDoux MS
中科院分区:
生物学3区
文献类型:
--
作者:
Xiao J;Khan MM;Vemula S;Tian J;LeDoux MS

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CIZ1 plays a role in DNA synthesis at the G1/S checkpoint. Ciz1 gene-trap null mice manifest motor dysfunction, cell-cycle abnormalities and DNA damage. In contrast, it has previously been reported that mouse embryonic fibroblasts derived from presumed Ciz1 knock-out mice (Ciz1 tm1.1Homy/tm1.1Homy) generated by crossing Cre-expressing mice with exon 5-floxed mice (Ciz1 tm1Homy/tm1Homy) do not exhibit evidence of enhanced DNA damage following γ-irradiation or cell-cycle defects. Here, we report that Ciz1 tm1.1Homy/tm1.1Homy mice show loss of Ciz1 exon 5 but are neurologically normal and express abnormal transcripts (Ciz1ΔE5/ΔE5 mice) that are translated into one or more proteins of approximate wild-type size. Therefore, Ciz1 tm1.1Homy/tm1.1Homy mice (Ciz1ΔE5/ΔE5) lose residues encoded by exon 5 but may gain function from novel amino acid sequences.
DOI: 10.1016/j.expneurol.2016.05.006
发表时间: 2016-09
影响因子: 5.3
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发表时间: 2010-11-01
期刊: GENETICS
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