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首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Xenopus pitx3 Target Genes lhx1 and xnr5 are Identified Using a Novel Three-fluor Flow Cytometry-based Analysis of Promoter Activation and Repression
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Xenopus pitx3 Target Genes lhx1 and xnr5 are Identified Using a Novel Three-fluor Flow Cytometry-based Analysis of Promoter Activation and Repression

机译:使用基于新的三氟流细胞术的启动子激活和抑制分析,鉴定出Xenopus pitx3靶基因LHX1和XNR5

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摘要

Background: Pitx3 plays a well understood role in directing development of lens, muscle fiber, and dopaminergic neurons; however, in Xenopus laevis, it may also play a role in early gastrulation and somitogenesis. Potential downstream targets of pitx3 possess multiple binding motifs that would not be readily accessible by conventional promoter analysis. Results: We isolated and characterized pitx3 target genes lhx1 and xnr5 using a novel three-fluor flow cytometry tool that was designed to dissect promoters with multiple binding sites for the same transcription factor. This approach was calibrated using a known pitx3 target gene, Tyrosine hydroxylase. Conclusions: We demonstrate how flow cytometry can be used to detect gene regulatory changes with exquisite precision on a cell-by-cell basis, and establish that in HEK293 cells, pitx3 directly activates lhx1 and represses xnr5. (C) 2017 Wiley Periodicals, Inc.
机译:背景:PITX3在引导镜头,肌纤维和多巴胺能神经元的发展方面发挥着理解的作用; 然而,在Xenopus Laevis中,它也可能在早期脱脂和同化体中发挥作用。 PITX3的潜在下游靶标具有多种结合基序,其不会通过常规启动子分析易于访问。 结果:使用新型三种氟流细胞术工具,我们分离和表征PitX3靶基因LHX1和XNR5,该工具被设计成将具有多个结合位点的促进剂置于相同的转录因子。 使用已知的PITX3靶基因,酪氨酸羟化酶校准该方法。 结论:我们证明了流式细胞术如何用于检测基因调节因细胞基础的精确精度,并在HEK293细胞中确定PITX3直接激活LHX1并抑制XNR5。 (c)2017 Wiley期刊,Inc。

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