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通过Gli3/Fgfs/ Gremlin确定指(趾)数量和身份需要融合抑制因子。

Suppressor of Fused Is Required for Determining Digit Number and Identity via Gli3/Fgfs/Gremlin.

作者信息

Li Jianying, Wang Qihui, Cui Ying, Yang Xueqin, Li Yan, Zhang Xiaoyun, Qiu Mengsheng, Zhang Ze, Zhang Zunyi

机构信息

Zhejiang Key Laboratory for Organogenesis and Regenerative technology, Institute of Developmental and Regenerative Biology, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China.

Zhejiang Key Laboratory for Organogenesis and Regenerative technology, Institute of Developmental and Regenerative Biology, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China; Department of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, Kentucky 40292, United States of America.

出版信息

PLoS One. 2015 May 22;10(5):e0128006. doi: 10.1371/journal.pone.0128006. eCollection 2015.

Abstract

The anterior-posterior patterning of the vertebrate limb bud requires closely coordinated signaling interactions, including Sonic Hedgehog (Shh)-mediated counteraction of the Gli3 transcription factor in the distal and posterior mesenchyme of the limb bud. Suppressor of Fused (Sufu), an intracellular negative regulator of Shh signaling via Gli2 and Gli3, is implicated in early development of the mouse limb bud. However, how Sufu is involved in the genetic regulation of limb bud patterning still remains elusive. In this study, we show that the conditional deletion of Sufu in the mesenchyme of the early limb bud results in polydactyly with loss of digit identity and supernumerary bones in the wrist and the ankle. These pattern alterations are associated with anterior expansion of HoxD genes located at the 5' end of the cluster. By focusing on gene expression analysis of Shh/Gremlin1/Fgf signaling critical for the establishment and maintenance of anterior-posterior patterning, we show that early response to loss of Sufu involves anterior prolongation of Fgf4 and Fgf8 expression in the apical ectodermal ridge at E10.5. We also reveal the anterior activation of Shh-dependent posterior markers Ptc1, Gli1 and Gremlin in limb buds lacking Sufu. Furthermore, we find that loss of Sufu leads to attenuated levels of repressor Gli2 and repressor Gli3 in the early limb bud. Moreover, expression of Hand2 is activated in the entire limb bud at the early outgrowth stage in the mutant lacking Sufu. Thus, we provide evidence that Sufu is involved in the genetic network that restricts the posterior expression of Gli2/3/Hand2 and Gremlin/Fgf in limb bud patterning.

摘要

脊椎动物肢芽的前后模式形成需要紧密协调的信号相互作用,包括音猬因子(Shh)介导的对肢芽远端和后间充质中Gli3转录因子的拮抗作用。融合抑制因子(Sufu)是一种通过Gli2和Gli3对Shh信号进行细胞内负调控的因子,与小鼠肢芽的早期发育有关。然而,Sufu如何参与肢芽模式形成的遗传调控仍不清楚。在本研究中,我们发现早期肢芽间充质中Sufu的条件性缺失会导致多指畸形,伴有指身份丧失以及腕部和踝部出现多余骨骼。这些模式改变与位于基因簇5'端的HoxD基因的前部扩展有关。通过聚焦于对前后模式形成的建立和维持至关重要的Shh/Gremlin1/Fgf信号的基因表达分析,我们发现对Sufu缺失的早期反应涉及E10.5时顶外胚层嵴中Fgf4和Fgf8表达的前部延长。我们还揭示了在缺乏Sufu的肢芽中,Shh依赖的后部标记物Ptc1、Gli1和Gremlin的前部激活。此外,我们发现Sufu的缺失导致早期肢芽中抑制性Gli2和抑制性Gli3水平降低。此外,在缺乏Sufu的突变体中,Hand2的表达在早期肢芽生长阶段的整个肢芽中被激活。因此,我们提供了证据表明Sufu参与了限制Gli2/3/Hand2和Gremlin/Fgf在肢芽模式形成中后部表达的遗传网络。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89b9/4441507/e3185d3ba424/pone.0128006.g001.jpg

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