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一个分离PLZF骨骼模式形成和精原细胞更新功能的等位基因。

An allele separating skeletal patterning and spermatogonial renewal functions of PLZF.

作者信息

Ching Yung-Hao, Wilson Lawriston A, Schimenti John C

机构信息

Department of Biomedical Sciences, Cornell University, Ithaca, NY 14850 USA.

出版信息

BMC Dev Biol. 2010 Mar 25;10:33. doi: 10.1186/1471-213X-10-33.

Abstract

BACKGROUND

The promyelocytic leukemia zinc finger gene Plzf (also called Zbtb16, Zfp145 or Green's luxoid) belongs to the POZ/zinc-finger family of transcription factors. It contains a BTB/POZ domain that mediates epigenetic transcriptional repression. PLZF is essential for proper skeleton patterning and male germ cell renewal. Two alleles have been reported that display similar phenotypes: a targeted knock-out, and the spontaneous nonsense mutation luxoid.

RESULTS

We describe a new ENU induced missense allele of Plzf called seven toes (Plzf7t). Homozygous animals exhibit hindlimb and axial skeleton abnormalities. Whereas the skeletal abnormalities are similar to those of the other alleles, Plzf7t differs in that it does not cause spermatogonial depletion and infertility. Positional cloning revealed a point mutation changing the evolutionarily conserved amino acid Glu44 to Gly, possibly altering the BTB domain's activity.

CONCLUSIONS

Plzf7t is a separation-of-function allele that reveals differential requirements for domains of PLZF in different developmental milieus.

摘要

背景

早幼粒细胞白血病锌指基因Plzf(也称为Zbtb16、Zfp145或格林氏类luxoid基因)属于转录因子的POZ/锌指家族。它包含一个介导表观遗传转录抑制的BTB/POZ结构域。PLZF对于正常的骨骼模式形成和雄性生殖细胞更新至关重要。已经报道了两个表现出相似表型的等位基因:一个靶向敲除等位基因,以及自发的无义突变luxoid。

结果

我们描述了一种新的由ENU诱导的Plzf错义等位基因,称为七趾(Plzf7t)。纯合动物表现出后肢和轴向骨骼异常。虽然骨骼异常与其他等位基因相似,但Plzf7t的不同之处在于它不会导致精原细胞耗竭和不育。定位克隆揭示了一个点突变,将进化上保守的氨基酸Glu44变为Gly,这可能改变了BTB结构域的活性。

结论

Plzf7t是一个功能分离等位基因,揭示了在不同发育环境中对PLZF结构域的不同需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba39/2859375/45b9628cfa8c/1471-213X-10-33-1.jpg

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