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平面细胞极性依赖的微管不对称组织,用于节点细胞中基体的极化定位。

Planar cell polarity-dependent asymmetric organization of microtubules for polarized positioning of the basal body in node cells.

作者信息

Sai Xiaorei, Ikawa Yayoi, Nishimura Hiromi, Mizuno Katsutoshi, Kajikawa Eriko, Katoh Takanobu A, Kimura Toshiya, Shiratori Hidetaka, Takaoka Katsuyoshi, Hamada Hiroshi, Minegishi Katsura

机构信息

Laboratory for Organismal Patterning, RIKEN Center for Biosystems Dynamics Research, Kobe, Hyogo 650-0047, Japan.

Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 560-0011, Japan.

出版信息

Development. 2022 May 1;149(9). doi: 10.1242/dev.200315. Epub 2022 May 6.

Abstract

For left-right symmetry breaking in the mouse embryo, the basal body must become positioned at the posterior side of node cells, but the precise mechanism for this has remained unknown. Here, we examined the role of microtubules (MTs) and actomyosin in this basal body positioning. Exposure of mouse embryos to agents that stabilize or destabilize MTs or F-actin impaired such positioning. Active myosin II was detected at the anterior side of node cells before the posterior shift of the basal body, and this asymmetric activation was lost in Prickle and dachsous mutant embryos. The organization of basal-body associated MTs (baMTs) was asymmetric between the anterior and posterior sides of node cells, with anterior baMTs extending horizontally and posterior baMTs extending vertically. This asymmetry became evident after polarization of the PCP core protein Vangl1 and before the posterior positioning of the basal body, and it also required the PCP core proteins Prickle and dachsous. Our results suggest that the asymmetry in baMT organization may play a role in correct positioning of the basal body for left-right symmetry breaking.

摘要

对于小鼠胚胎中的左右对称打破,基体必须定位在节点细胞的后侧,但具体机制尚不清楚。在此,我们研究了微管(MTs)和肌动球蛋白在这种基体定位中的作用。将小鼠胚胎暴露于稳定或破坏MTs或F-肌动蛋白的试剂中会损害这种定位。在基体向后移动之前,在节点细胞的前侧检测到活性肌球蛋白II,而这种不对称激活在Prickle和dachsous突变胚胎中消失。基体相关微管(baMTs)的组织在节点细胞的前后侧之间是不对称的,前侧baMTs水平延伸,后侧baMTs垂直延伸。这种不对称在PCP核心蛋白Vangl1极化后且基体向后定位之前变得明显,并且它也需要PCP核心蛋白Prickle和dachsous。我们的结果表明,baMT组织的不对称可能在基体的正确定位以实现左右对称打破中起作用。

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