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张欣, 张祺, 潘军, 周建峰, 白艳, 荣小至. Rspo1调控斑马鱼胚胎汇聚延伸运动的研究[J]. 水生生物学报, 2023, 47(2): 298-307. DOI: 10.7541/2023.2022.0095
引用本文: 张欣, 张祺, 潘军, 周建峰, 白艳, 荣小至. Rspo1调控斑马鱼胚胎汇聚延伸运动的研究[J]. 水生生物学报, 2023, 47(2): 298-307. DOI: 10.7541/2023.2022.0095
ZHANG Xin, ZHANG Qi, PAN Jun, ZHOU Jian-Feng, BAI Yan, RONG Xiao-Zhi. RSPO1 IN MODULATING CONVERGENCE AND EXTENSION MOVEMENT IN ZEBRAFISH EMBRYOS[J]. ACTA HYDROBIOLOGICA SINICA, 2023, 47(2): 298-307. DOI: 10.7541/2023.2022.0095
Citation: ZHANG Xin, ZHANG Qi, PAN Jun, ZHOU Jian-Feng, BAI Yan, RONG Xiao-Zhi. RSPO1 IN MODULATING CONVERGENCE AND EXTENSION MOVEMENT IN ZEBRAFISH EMBRYOS[J]. ACTA HYDROBIOLOGICA SINICA, 2023, 47(2): 298-307. DOI: 10.7541/2023.2022.0095

Rspo1调控斑马鱼胚胎汇聚延伸运动的研究

RSPO1 IN MODULATING CONVERGENCE AND EXTENSION MOVEMENT IN ZEBRAFISH EMBRYOS

  • 摘要: Rspo1 (R-spondin 1)是分泌型Rspos (R-spondins)蛋白家族的成员, 在雌性发育、血管生成和癌症等多个方面具有调控作用。为了研究Rspo1在早期胚胎发育中的功能, 以斑马鱼(Danio rerio)作为模式生物, 利用反转录PCR及原位杂交技术检测rspo1基因的时空表达模式; 通过显微注射rspo1 mRNA或rspo1反义寡核苷酸(Morpholino, MO)对rspo1进行过表达或敲降; 通过形态观察及原位杂交技术检测胚胎汇聚延伸(Convergence and extension, CE)运动是否正常; 利用荧光素酶活性检测实验测定Wnt/PCP信号通路活性水平; 通过蛋白印迹法检测表征Wnt/PCP信号通路活性的磷酸化JNK (Jun N-terminal kinase)蛋白的水平。结果显示: rspo1为母源基因, 在12hpf前胚胎中呈全身性表达, rspo1的过表达或敲降均影响胚胎的CE运动; 过表达rspo1降低Wnt/PCP信号通路报告质粒的活性, 而敲降rspo1则增加其活性, 与之相一致, rspo1敲降的胚胎中磷酸化JNK的水平显著升高; 此外, rspo1 mRNA与dnJNK (Dominant negative JNK) mRNA的共同注射, 以及rspo1 MOs与wnt11wnt5b mRNA的共同注射均能协同诱导CE运动缺陷。综上, 在斑马鱼胚胎中, Rspo1通过负调控Wnt/PCP信号通路来调控胚胎的汇聚延伸运动。

     

    Abstract: In vertebrate embryos, gastrulation is the fundamental morphogenetic movements. It leads to the formation of the basic germ layers and the body axis. During gastrulation, convergence and extension (CE) movements narrow a group of cells mediolaterally and lengthen them to facilitate the elongation of the anteroposterior axis. In this process, the planar cell polarity (PCP) pathway, also called the noncanonical Wnt signaling pathway, is of particular importance to control CE movements. However, the precise cellular and molecular mechanisms underlying this process remains to be further studied. Rspo1 (R-spondin 1) is a secreted protein that has been implicated in activating the Wnt/β-catenin signaling levels with Wnt ligands, through which Rspo1 promotes angiogenesis and specifies hematopoietic stem cells, as well as promotes female development. Recently, it was reported that Rspo1 exhibits Wnt/β-catenin independent roles. For example, Rspo1-Lgr4-cAMP-Erα axis regulates estrogen receptor expression, and RSPO1-LGR5 activates TGFβ signaling in colon cancer. Given the complex role of Rspo1, we speculate that Rspo1 is involved in the early embryonic development. To investigate the developmental role of Rspo1 in zebrafish embryos, we examined the spatiotemporal expression pattern of rspo1 using RT-PCR and whole-mount in situ hybridization. The results showed that rspo1 mRNA is maternally deposited and expresses ubiquitously in early embryonic stages before 12hpf (hours post fertilization), implying that Rspo1 may play an important role in the regulation of embryonic development. Next, we carried out gain-of-function and loss-of function analysis of Rspo1. The results showed that either overexpression or knockdown of rspo1 abrogates the CE movements during gastrulation. In order to explore whether rspo1 affects CE movement by participating in Wnt/PCP signaling pathway, we used AP-1 luciferase reporter to monitor Wnt/PCP in zebrafish embryos. The results showed that forced expression of rspo1 decreases but knockdown of rspo1 increases Wnt/PCP signaling reporter activity, indicating that Rspo1 inhibits Wnt/PCP signaling pathway. Consistent with this result, the phosphorylated-JNK levels, an indicator of activity of Wnt/PCP signaling pathway, dramatically increased in rspo1 morphant embryos at gastrulation stage. Further analyses indicate that coinjection of rspo1 mRNA and dnJNK (Dominant negative JNK) mRNA, or coinjection of rspo1 MOs and wnt11/wnt5b mRNA synergistically enhanced CE defects. Taken together, these results suggest that Rspo1 regulates CE movements during gastrulation by negatively regulating the Wnt/PCP signaling in zebrafish embryos. Overall, our studies will provide novel insights into the regulation of Wnt/PCP signaling in vertebrates.

     

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