Literature DB >> 35390280

Enhanced lipogenesis through Pparγ helps cavefish adapt to food scarcity.

Shaolei Xiong1, Wei Wang2, Alexander Kenzior1, Luke Olsen3, Jaya Krishnan1, Jenna Persons1, Kyle Medley1, Robert Peuß4, Yongfu Wang1, Shiyuan Chen1, Ning Zhang1, Nancy Thomas1, John M Miles5, Alejandro Sánchez Alvarado6, Nicolas Rohner7.   

Abstract

Nutrient availability varies seasonally and spatially in the wild. While many animals, such as hibernating animals or migrating birds, evolved strategies to overcome periods of nutrient scarcity,1,2 the cellular mechanisms of these strategies are poorly understood. Cave environments represent an example of nutrient-deprived environments, since the lack of sunlight and therefore primary energy production drastically diminishes the nutrient availability.3 Here, we used Astyanax mexicanus, which includes river-dwelling surface fish and cave-adapted cavefish populations, to study the genetic adaptation to nutrient limitations.4-9 We show that cavefish populations store large amounts of fat in different body regions when fed ad libitum in the lab. We found higher expression of lipogenesis genes in cavefish livers when fed the same amount of food as surface fish, suggesting an improved ability of cavefish to use lipogenesis to convert available energy into triglycerides for storage into adipose tissue.10-12 Moreover, the lipid metabolism regulator, peroxisome proliferator-activated receptor γ (Pparγ), is upregulated at both transcript and protein levels in cavefish livers. Chromatin immunoprecipitation sequencing (ChIP-seq) showed that Pparγ binds cavefish promoter regions of genes to a higher extent than surface fish and inhibiting Pparγ in vivo decreases fat accumulation in A. mexicanus. Finally, we identified nonsense mutations in per2, a known repressor of Pparγ, providing a possible regulatory mechanism of Pparγ in cavefish. Taken together, our study reveals that upregulated Pparγ promotes higher levels of lipogenesis in the liver and contributes to higher body fat accumulation in cavefish populations, an important adaptation to nutrient-limited environments.
Copyright © 2022 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Astyanax mexicanus; adaptation; cavefish; fat storage; lipid metabolism; lipogenesis; per2; pparγ

Mesh:

Substances:

Year:  2022        PMID: 35390280      PMCID: PMC9133166          DOI: 10.1016/j.cub.2022.03.038

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.900


  49 in total

1.  A simple method for the isolation and purification of total lipides from animal tissues.

Authors:  J FOLCH; M LEES; G H SLOANE STANLEY
Journal:  J Biol Chem       Date:  1957-05       Impact factor: 5.157

Review 2.  Review: Peroxisome proliferator-activated receptor gamma and adipose tissue--understanding obesity-related changes in regulation of lipid and glucose metabolism.

Authors:  Arya M Sharma; Bart Staels
Journal:  J Clin Endocrinol Metab       Date:  2006-12-05       Impact factor: 5.958

3.  Insulin resistance in cavefish as an adaptation to a nutrient-limited environment.

Authors:  Misty R Riddle; Ariel C Aspiras; Karin Gaudenz; Robert Peuß; Jenny Y Sung; Brian Martineau; Megan Peavey; Andrew C Box; Julius A Tabin; Suzanne McGaugh; Richard Borowsky; Clifford J Tabin; Nicolas Rohner
Journal:  Nature       Date:  2018-03-21       Impact factor: 49.962

4.  FIMO: scanning for occurrences of a given motif.

Authors:  Charles E Grant; Timothy L Bailey; William Stafford Noble
Journal:  Bioinformatics       Date:  2011-02-16       Impact factor: 6.937

5.  rtracklayer: an R package for interfacing with genome browsers.

Authors:  Michael Lawrence; Robert Gentleman; Vincent Carey
Journal:  Bioinformatics       Date:  2009-05-25       Impact factor: 6.937

6.  BEDTools: a flexible suite of utilities for comparing genomic features.

Authors:  Aaron R Quinlan; Ira M Hall
Journal:  Bioinformatics       Date:  2010-01-28       Impact factor: 6.937

7.  Hepatic fatty acid transporter Cd36 is a common target of LXR, PXR, and PPARgamma in promoting steatosis.

Authors:  Jie Zhou; Maria Febbraio; Taira Wada; Yonggong Zhai; Ramalinga Kuruba; Jinhan He; Jung Hoon Lee; Shaheen Khadem; Songrong Ren; Song Li; Roy L Silverstein; Wen Xie
Journal:  Gastroenterology       Date:  2007-11-28       Impact factor: 22.682

Review 8.  PPARγ signaling and metabolism: the good, the bad and the future.

Authors:  Maryam Ahmadian; Jae Myoung Suh; Nasun Hah; Christopher Liddle; Annette R Atkins; Michael Downes; Ronald M Evans
Journal:  Nat Med       Date:  2013-05-07       Impact factor: 53.440

9.  Desaturation index versus isotopically measured de novo lipogenesis as an indicator of acute systemic lipogenesis.

Authors:  Scott V Harding; Kevin P Bateman; Brian P Kennedy; Todd C Rideout; Peter J H Jones
Journal:  BMC Res Notes       Date:  2015-02-23

10.  PPAR gamma 2 prevents lipotoxicity by controlling adipose tissue expandability and peripheral lipid metabolism.

Authors:  Gema Medina-Gomez; Sarah L Gray; Laxman Yetukuri; Kenju Shimomura; Sam Virtue; Mark Campbell; R Keira Curtis; Mercedes Jimenez-Linan; Margaret Blount; Giles S H Yeo; Miguel Lopez; Tuulikki Seppänen-Laakso; Frances M Ashcroft; Matej Oresic; Antonio Vidal-Puig
Journal:  PLoS Genet       Date:  2007-04-27       Impact factor: 5.917

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  2 in total

1.  How a cave-dwelling fish stores fat through feast and famine.

Authors: 
Journal:  Nature       Date:  2022-04       Impact factor: 49.962

2.  Liver-derived cell lines from cavefish Astyanax mexicanus as an in vitro model for studying metabolic adaptation.

Authors:  Jaya Krishnan; Yan Wang; Olga Kenzior; Huzaifa Hassan; Luke Olsen; Dai Tsuchiya; Alexander Kenzior; Robert Peuß; Shaolei Xiong; Yongfu Wang; Chongbei Zhao; Nicolas Rohner
Journal:  Sci Rep       Date:  2022-06-16       Impact factor: 4.996

  2 in total

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