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Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish.

Authors :
Lam, Sin Man
Li, Jie
Sun, Huan
Mao, Weining
Lu, Zongmin
Zhao, Qingshuo
Han, Chao
Gong, Xia
Jiang, Binhua
Chua, Gek Huey
Zhao, Zhenwen
Meng, Fanwei
Shui, Guanghou
Source :
Molecular Biology & Evolution; Apr2022, Vol. 39 Issue 4, p1-18, 18p
Publication Year :
2022

Abstract

Sinocyclocheilus represents a rare, freshwater teleost genus endemic to China that comprises the river-dwelling surface fish and the cave-dwelling cavefish. Using a combinatorial approach of quantitative lipidomics and mass-spectrometry imaging (MSI), we demonstrated that neural compartmentalization of lipid distribution and lipid metabolism is associated with the evolution of troglomorphic traits in Sinocyclocheilus. Attenuated docosahexaenoic acid (DHA) biosynthesis via the Δ4 desaturase pathway led to reductions in DHA-phospholipids in cavefish cerebellum. Instead, cavefish accumulates arachidonic acid-phospholipids that may disfavor retinotectal arbor growth. Importantly, MSI of sulfatides coupled with immunostaining of myelin basic protein and transmission electron microscopy images of hindbrain axons revealed demyelination in cavefish raphe serotonergic neurons. Demyelination in cavefish parallels the loss of neuroplasticity governing social behavior such as aggressive dominance. Outside the brain, quantitative lipidomics and qRT-PCR revealed systemic reductions in membrane esterified DHAs in the liver, attributed to suppression of genes along the Sprecher pathway (elovl2 , elovl5 , and acox1). Development of fatty livers was observed in cavefish; likely mediated by an impeded mobilization of storage lipids, as evident in the diminished expressions of pnpla2 , lipea , lipeb , dagla , and mgll ; and suppressed β-oxidation of fatty acyls via both mitochondria and peroxisomes as reflected in the reduced expressions of cpt1ab , hadhaa , cpt2 , decr1, and acox1. These neurological and systemic metabolic adaptations serve to reduce energy expenditure, forming the basis of recessive evolution that eliminates nonessential morphological and behavioral traits and giving cavefish a selective advantage to thrive in caves where proper resource allocation becomes a major determinant of survival. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07374038
Volume :
39
Issue :
4
Database :
Complementary Index
Journal :
Molecular Biology & Evolution
Publication Type :
Academic Journal
Accession number :
156630781
Full Text :
https://doi.org/10.1093/molbev/msac050