Genome-wide screening of NEAT1 regulators reveals cross-regulation between paraspeckles and mitochondria

• Published in: Nature cell biology Vol. 20; no. 10; pp. 1145 - 1158
• Main Authors: Wang, Yang, Hu, Shi-Bin, Wang, Meng-Ran, Yao, Run-Wen, Wu, Di, Yang, Li, Chen, Ling-Ling
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01.10.2018
• Subjects: Activating Transcription Factor 2 - genetics; Activating Transcription Factor 2 - metabolism; Cell Nucleus - genetics; Cell Nucleus - metabolism; Depletion; Fluorescence; Gene expression; Gene Expression Profiling - methods; Genome, Human; Genomes; Green fluorescent protein; Green Fluorescent Proteins - genetics; Green Fluorescent Proteins - metabolism; HEK293 Cells; HeLa Cells; Humans; Mitochondria; Mitochondria - genetics; Mitochondria - metabolism; Morphology; Mutation; Proteins; Regulators; Ribonucleic acid; RNA; RNA Interference; RNA, Long Noncoding - genetics; RNA, Long Noncoding - isolation & purification; RNA-mediated interference; Transcription
• ISSN: 1465-7392; 1476-4679
• DOI: 10.1038/s41556-018-0204-2

The long noncoding RNA NEAT1 (nuclear enriched abundant transcript 1) nucleates the formation of paraspeckles, which constitute a type of nuclear body with multiple roles in gene expression. Here we identify NEAT1 regulators using an endogenous NEAT1 promoter-driven enhanced green fluorescent protein reporter in human cells coupled with genome-wide RNAi screens. The screens unexpectedly yield gene candidates involved in mitochondrial functions as essential regulators of NEAT1 expression and paraspeckle formation. Depletion of mitochondrial proteins and treatment of mitochondrial stressors both lead to aberrant NEAT1 expression via ATF2 as well as altered morphology and numbers of paraspeckles. These changes result in enhanced retention of mRNAs of nuclear-encoded mitochondrial proteins (mito-mRNAs) in paraspeckles. Correspondingly, NEAT1 depletion has profound effects on mitochondrial dynamics and function by altering the sequestration of mito-mRNAs in paraspeckles. Overall, our data provide a rich resource for understanding NEAT1 and paraspeckle regulation, and reveal a cross-regulation between paraspeckles and mitochondria.