人T细胞转录动力学、RNA定位和命运的单分子成像。

IF 8.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
M Valeria Lattanzio, Nikolina Šoštarić, Nandhini Kanagasabesan, Branka Popović, Antonia Bradarić, Leyma Wardak, Aurélie Guislain, Philipp Savakis, Evelina Tutucci, Monika C Wolkers
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引用次数: 0

摘要

T细胞是对抗感染和恶性肿瘤的关键效应细胞。为了达到这个目的,它们产生促炎细胞因子,包括IFN-γ和TNF。细胞因子的产生是一个受到严格调控的过程,但转录和转录后调控对mRNA表达的相对贡献尚不清楚。我们优化了用于原代人T细胞(T细胞smFISH)的单分子FISH,以同时定量新生RNA、成熟mRNA水平及其单细胞分辨率的定位。t细胞smFISH揭示了异质性的细胞因子mRNA水平,高细胞因子产生者显示双等位基因IFNG/TNF RNA转录活性。在整个激活过程中,细胞核细胞因子mRNA积累,而细胞质细胞因子mRNA通过翻译依赖性衰变降解。最后,t细胞smFISH发现了rna结合蛋白HuR对细胞因子的特异性调控。因此,T细胞smFISH为T细胞复杂的转录过程(后)提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-molecule imaging of transcription dynamics, RNA localization and fate in human T cells.

T cells are critical effector cells counteracting infections and malignancies. To achieve this, they produce pro-inflammatory cytokines, including IFN-γ and TNF. Cytokine production is a tightly regulated process, but the relative contribution of transcriptional and post-transcriptional regulation to mRNA expression remains unknown. We optimized single-molecule FISH for primary human T cells (T-cell smFISH) to simultaneously quantify nascent RNA, levels of mature mRNA, and its localization with single-cell resolution. T-cell smFISH uncovered heterogeneous cytokine mRNA levels, with high cytokine producers displaying biallelic IFNG/TNF RNA transcription activity. Throughout activation, nuclear cytokine mRNAs accumulated, whereas cytoplasmic cytokine mRNA was degraded through translation-dependent decay. Lastly, T-cell smFISH uncovered cytokine-specific regulation by the RNA-binding protein HuR. Thus, T-cell smFISH provides novel insights in the intricate (post)-transcriptional processes in T cells.

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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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