In vivo movement of retinoblastoma-related protein (RBR) towards cytoplasm during mitosis in Arabidopsisthaliana.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-07 DOI:10.1016/j.diff.2024.100800
Sergio Miguel-Hernández, Estephania Zluhan-Martínez, Adriana Garay-Arroyo, Lourdes Cabrera-Muñoz, Adriana Hernández-Angeles, Noé Valentín Durán-Figueroa, Vadim Pérez-Koldenkova, M Verónica Ponce-Castañeda
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Abstract

Retinoblastoma protein is central in signaling networks of fundamental cell decisions such as proliferation and differentiation in all metazoans and cancer development. Immunostaining and biochemical evidence demonstrated that during interphase retinoblastoma protein is in the nucleus and is hypophosphorylated, and during mitosis is in the cytoplasm and is hyperphosphorylated. The purpose of this study was to visualize in vivo in a non-diseased tissue, the dynamic spatial and temporal nuclear exit toward the cytoplasm of this protein during mitosis and its return to the nucleus to obtain insights into its potential cytosolic functions. Using high-resolution time-lapse images from confocal microscopy, we tracked in vivo the ortholog in plants the RETINOBLASTOMA RELATED (RBR) protein tagged with Green Fluorescent Protein (GFP) in Arabidopsis thaliana's root. RBR protein exits from dense aggregates in the nucleus before chromosomes are in prophase in less than 2 min, spreading outwards as smaller particles projected throughout the cytosol during mitosis like a diffusive yet controlled event until telophase, when the daughter's nuclei form; RBR returns to the nuclei in coordination with decondensing chromosomal DNA forming new aggregates again in punctuated larger structures in each corresponding nuclei. We propose RBR diffused particles in the cytoplasm may function as a cytosolic sensor of incoming signals, thus coordinating re-aggregation with DNA is a mechanism by which any new incoming signals encountered by RBR may lead to a reconfiguration of the nuclear transcriptomic context. The small RBR diffused particles in the cytoplasm may preserve topologic-like properties allowing them to aggregate and restore their nuclear location, they may also be part of transient cytoplasmic storage of the cellular pre-mitotic transcriptional context, that once inside the nuclei may execute both the pre mitosis transcriptional context as well as new transcriptional instructions.

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拟南芥有丝分裂过程中视网膜母细胞瘤相关蛋白(RBR)向细胞质的体内移动。
视网膜母细胞瘤蛋白在所有变态类动物的细胞增殖和分化以及癌症发展等基本细胞决定的信号网络中起着核心作用。免疫染色和生化证据表明,在细胞间期,视网膜母细胞瘤蛋白位于细胞核内,磷酸化程度低;而在有丝分裂期,视网膜母细胞瘤蛋白位于细胞质内,磷酸化程度高。本研究的目的是在非病变组织中,在体内观察该蛋白在有丝分裂过程中向细胞质的动态空间和时间核出口及其返回细胞核的过程,以深入了解其潜在的细胞膜功能。利用共聚焦显微镜拍摄的高分辨率延时图像,我们在拟南芥根部追踪了植物中的同源物--标记有绿色荧光蛋白(GFP)的RETINOBLASTOMA RELATED(RBR)蛋白。RBR 蛋白在染色体进入前期前不到 2 分钟就从细胞核的致密聚集体中流出,在有丝分裂过程中以更小的颗粒向外扩散,投射到整个细胞质中,就像一个扩散但可控的事件,直到端期,当子核形成时;RBR 与染色体 DNA 的解聚协调返回细胞核,在每个相应的细胞核中再次形成新的聚集体,形成点状的更大的结构。我们认为,细胞质中的 RBR 扩散颗粒可能充当了传入信号的细胞传感器,因此与 DNA 的重新聚集协调是一种机制,RBR 遇到的任何新传入信号都可能导致核转录组背景的重新配置。细胞质中扩散的 RBR 小颗粒可能保留了类似拓扑学的特性,使其能够聚集并恢复其核位置,它们也可能是细胞质中瞬时储存的有丝分裂前转录背景的一部分,一旦进入细胞核,就可能执行有丝分裂前转录背景以及新的转录指令。
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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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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