A Regulator of Metabolic Reprogramming: MicroRNA Let-7

Let-7, a gene firstly known to control the timing of Caenorhabditis elegans larval development does not code for a protein but instead produces small non-coding RNAs, microRNAs. Higher animals have multiple isoforms of mature let-7 microRNAs. Mature let-7 family members share the same “seed sequence...

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Main Author: Shuai Jiang
Format: Article
Language:English
Published: Elsevier 2019-07-01
Series:Translational Oncology
Online Access:http://www.sciencedirect.com/science/article/pii/S1936523319301652
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spelling doaj-429ca1009a2440afb7151421272a65702020-11-24T20:56:09ZengElsevierTranslational Oncology1936-52332019-07-0112710051013A Regulator of Metabolic Reprogramming: MicroRNA Let-7Shuai Jiang0Address all correspondence to: Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USALet-7, a gene firstly known to control the timing of Caenorhabditis elegans larval development does not code for a protein but instead produces small non-coding RNAs, microRNAs. Higher animals have multiple isoforms of mature let-7 microRNAs. Mature let-7 family members share the same “seed sequence” and distinct from each other slightly by ‘non-seed’ sequence region. Let-7 has emerged as a central regulator of systemic energy homeostasis and it displays remarkable plasticity in metabolic responses to nutrients availability and physiological activities. In this review, we discuss recent studies highlighting post-transcriptional mechanisms that govern metabolic reprogramming in distinct cells by let-7. We focus on the participation of the let-7 clusters in immune cells, and suggest that tissue-specific regulation of the let-7 clusters by engineered mouse models might impact metabolic homeostasis and will be required to elucidate their physiological and pathological roles in the in vivo disease models.http://www.sciencedirect.com/science/article/pii/S1936523319301652
collection DOAJ
language English
format Article
sources DOAJ
author Shuai Jiang
spellingShingle Shuai Jiang
A Regulator of Metabolic Reprogramming: MicroRNA Let-7
Translational Oncology
author_facet Shuai Jiang
author_sort Shuai Jiang
title A Regulator of Metabolic Reprogramming: MicroRNA Let-7
title_short A Regulator of Metabolic Reprogramming: MicroRNA Let-7
title_full A Regulator of Metabolic Reprogramming: MicroRNA Let-7
title_fullStr A Regulator of Metabolic Reprogramming: MicroRNA Let-7
title_full_unstemmed A Regulator of Metabolic Reprogramming: MicroRNA Let-7
title_sort regulator of metabolic reprogramming: microrna let-7
publisher Elsevier
series Translational Oncology
issn 1936-5233
publishDate 2019-07-01
description Let-7, a gene firstly known to control the timing of Caenorhabditis elegans larval development does not code for a protein but instead produces small non-coding RNAs, microRNAs. Higher animals have multiple isoforms of mature let-7 microRNAs. Mature let-7 family members share the same “seed sequence” and distinct from each other slightly by ‘non-seed’ sequence region. Let-7 has emerged as a central regulator of systemic energy homeostasis and it displays remarkable plasticity in metabolic responses to nutrients availability and physiological activities. In this review, we discuss recent studies highlighting post-transcriptional mechanisms that govern metabolic reprogramming in distinct cells by let-7. We focus on the participation of the let-7 clusters in immune cells, and suggest that tissue-specific regulation of the let-7 clusters by engineered mouse models might impact metabolic homeostasis and will be required to elucidate their physiological and pathological roles in the in vivo disease models.
url http://www.sciencedirect.com/science/article/pii/S1936523319301652
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