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排除发育中小鼠眼睛的Pax2调控元件的基因组位置。

Excluding the Genomic Location of Pax2 Regulatory Elements for the Developing Mouse Eye.

作者信息

Ho Tzu-Hua, Santamaria-Munoz Daniela, Hamelynck Hollin, La Torre Anna, Glaser Tom, Brown Nadean L

机构信息

Department of Cell Biology and Human Anatomy, University of California, Davis, California, USA.

出版信息

Genesis. 2025 Apr;63(2):e70016. doi: 10.1002/dvg.70016.

Abstract

The Pax2 transcription factor is activated uniformly in the optic vesicle/cup, but becomes progressively restricted to the forming optic disc and stalk. In the eye, it is not known how Pax2 expression is regulated and progressively restricted, in part because no Pax2 regulatory elements have been identified for this organ. Multiple Pax2-Cre mouse transgenic lines have been produced, but essentially none of these Cre recombinase drivers are active in the visual system. Only Tg(BAC-Pax2-cre) mice have been reported to express Cre in a subset of postnatal retinal astrocytes. We confirm this observation and demonstrate ectopic expression in branchial arches, extraocular muscles, and a subset of GABAergic amacrine cells. Our findings suggest that major eye enhancer(s) for mouse Pax2 reside outside the > 180 kb genomic segment delimited by Pax2 BAC transgenes.

摘要

Pax2转录因子在视泡/视杯中均匀激活,但逐渐局限于正在形成的视盘和视柄。在眼睛中,Pax2的表达是如何被调控并逐渐受到限制的尚不清楚,部分原因是尚未鉴定出该器官的Pax2调控元件。已经产生了多个Pax2-Cre小鼠转基因品系,但基本上这些Cre重组酶驱动子在视觉系统中均无活性。据报道,只有Tg(BAC-Pax2-cre)小鼠在出生后视网膜星形胶质细胞的一个亚群中表达Cre。我们证实了这一观察结果,并证明其在鳃弓、眼外肌和一部分γ-氨基丁酸能无长突细胞中有异位表达。我们的研究结果表明,小鼠Pax2的主要眼部增强子位于由Pax2 BAC转基因界定的>180 kb基因组片段之外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6c7/12040291/946723f4d30b/DVG-63-e70016-g001.jpg

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