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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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 |
work_keys_str_mv |
AT shuaijiang aregulatorofmetabolicreprogrammingmicrornalet7 AT shuaijiang regulatorofmetabolicreprogrammingmicrornalet7 |
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