对比ISL1和LHX3的dna结合行为,是神经元细胞分化基因靶向的基础

IF 3.5 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Structural Biology: X Pub Date : 2021-01-01 DOI:10.1016/j.yjsbx.2020.100043
Ngaio C. Smith , Lorna E. Wilkinson-White , Ann H.Y. Kwan , Jill Trewhella , Jacqueline M. Matthews
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引用次数: 1

摘要

ISL1和LHX3在脊髓运动神经元发育中的作用已被证实。虽然LHX3触发分化为中间神经元,但在发育中的神经元细胞中额外表达ISL1足以将其发育轨迹转向脊髓运动神经元。然而,这些转录因子作用的潜在机制尚不清楚。在这里,我们使用了电泳迁移位移测定(EMSAs)和表面等离子体共振(SPR)来探测这两种蛋白的不同dna结合行为,无论是单独的还是在模拟发育中的神经元中发现的复合物中,发现ISL1与LHX3的结合特性明显不同。我们使用小角度x射线散射(SAXS)对含有ISL1和LHX3的dna结合物种进行结构表征。综上所述,这些结果使我们能够建立一个模型,说明这两个dna结合模块如何协调调节基因表达和指导脊髓运动神经元的发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Contrasting DNA-binding behaviour by ISL1 and LHX3 underpins differential gene targeting in neuronal cell specification

The roles of ISL1 and LHX3 in the development of spinal motor neurons have been well established. Whereas LHX3 triggers differentiation into interneurons, the additional expression of ISL1 in developing neuronal cells is sufficient to redirect their developmental trajectory towards spinal motor neurons. However, the underlying mechanism of this action by these transcription factors is less well understood. Here, we used electrophoretic mobility shift assays (EMSAs) and surface plasmon resonance (SPR) to probe the different DNA-binding behaviours of these two proteins, both alone and in complexes mimicking those found in developing neurons, and found that ISL1 shows markedly different binding properties to LHX3. We used small angle X-ray scattering (SAXS) to structurally characterise DNA-bound species containing ISL1 and LHX3. Taken together, these results have allowed us to develop a model of how these two DNA-binding modules coordinate to regulate gene expression and direct development of spinal motor neurons.

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来源期刊
Journal of Structural Biology: X
Journal of Structural Biology: X Biochemistry, Genetics and Molecular Biology-Structural Biology
CiteScore
6.50
自引率
0.00%
发文量
20
审稿时长
62 days
期刊最新文献
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