酶介导的接近标记揭示了DLGAP5 mRNA在有丝分裂过程中对中心体的共翻译靶向。

IF 3.1 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Gang Wang, Mo Li and Peng Zou
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引用次数: 0

摘要

亚细胞RNA定位是真核细胞中的一种保守机制,在细胞增殖、分化和胚胎发育等多种生理过程中起着关键作用。然而,由于技术上的困难,中心体定位mrna的表征仍未得到充分探索。在这项研究中,我们利用apex2介导的接近标记来绘制中心体-近端转录组,鉴定出DLGAP5 mRNA是有丝分裂过程中中心体定位的新转录物。通过药物干扰、截断、删除和诱变的组合,我们证明了新生MBD1多肽的微管结合是DLGAP5 mRNA中心体运输所必需的。我们的数据还显示mRNA靶向效率与编码序列(CDS)长度密切相关。因此,我们的研究为未来中心体定位rna的研究提供了转录组学资源,并揭示了mRNA中心体定位的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enzyme-mediated proximity labeling reveals the co-translational targeting of DLGAP5 mRNA to the centrosome during mitosis†

Enzyme-mediated proximity labeling reveals the co-translational targeting of DLGAP5 mRNA to the centrosome during mitosis†

Subcellular RNA localization is a conserved mechanism in eukaryotic cells and plays critical roles in diverse physiological processes including cell proliferation, differentiation, and embryo development. Nevertheless, the characterization of centrosome-localized mRNAs remains underexplored due to technical difficulties. In this study, we utilize APEX2-mediated proximity labeling to map the centrosome-proximal transcriptome, identifying DLGAP5 mRNA as a novel centrosome-localized transcript during mitosis. Using a combination of drug perturbation, truncation, deletion, and mutagenesis, we demonstrate that microtubule binding of nascent MBD1 polypeptides is required for centrosomal transport of DLGAP5 mRNA. Our data also reveal that mRNA targeting efficiency is tightly linked to the coding sequence (CDS) length. Thus, our study provides a transcriptomic resource for future investigation of centrosome-localized RNAs and sheds light on mechanisms underlying mRNA centrosomal localization.

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来源期刊
CiteScore
6.10
自引率
0.00%
发文量
128
审稿时长
10 weeks
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