scispace - formally typeset
Open AccessJournal ArticleDOI

Lipid and Carbohydrate Metabolism in Caenorhabditis Elegans

Jennifer L. Watts, +1 more
- 01 Oct 2017 - 
- Vol. 207, Iss: 2, pp 413-446
TLDR
This review outlines lipid and carbohydrate structures as well as biosynthesis and breakdown pathways that have been characterized in C. elegans and brings attention to functional studies using mutant strains that reveal physiological roles for specific lipids and carbohydrates during development, aging, and adaptation to changing environmental conditions.
Abstract
Lipid and carbohydrate metabolism are highly conserved processes that affect nearly all aspects of organismal biology. Caenorhabditis elegans eat bacteria, which consist of lipids, carbohydrates, and proteins that are broken down during digestion into fatty acids, simple sugars, and amino acid precursors. With these nutrients, C. elegans synthesizes a wide range of metabolites that are required for development and behavior. In this review, we outline lipid and carbohydrate structures as well as biosynthesis and breakdown pathways that have been characterized in C. elegans We bring attention to functional studies using mutant strains that reveal physiological roles for specific lipids and carbohydrates during development, aging, and adaptation to changing environmental conditions.

read more

Citations
More filters
Journal ArticleDOI

TOR Signaling in Caenorhabditis elegans Development, Metabolism, and Aging.

TL;DR: The state of the TOR field in C. elegans is reviewed, and what is learned about its functions in development, metabolism, and aging is focused on.
Journal ArticleDOI

WormCat: An Online Tool for Annotation and Visualization of Caenorhabditis elegans Genome-Scale Data

TL;DR: WormCat, a web-based tool that uses a near-complete annotation of the C. elegans genome to identify coexpressed gene sets and scaled heat map for enrichment visualization, is developed and tested, showing that it reproduces major categories identified by GO.
Journal ArticleDOI

Immunometabolic Crosstalk: An Ancestral Principle of Trained Immunity?

TL;DR: Evidence is discussed from C. elegans and murine/human systems supporting the concept of an ancestral principle regulating innate immune memory by controlling cellular metabolism, posit that changes in cellular metabolism may be a common denominator of innateimmune memory from lower animals to mammals.
Journal ArticleDOI

Biology of the Caenorhabditis elegans Germline Stem Cell System.

TL;DR: C. elegans is a powerful model for understanding germline stem cells and stem cell biology and the Notch regulated genetic network that controls the key decision between the stem cell fate and meiotic development occurs under optimal laboratory conditions in adult and larval stages.
Journal ArticleDOI

Natural variation in C. elegans arsenic toxicity is explained by differences in branched chain amino acid metabolism.

TL;DR: This study implicates the BCKDH complex and BCAA metabolism in arsenic responses, demonstrating the power of C. elegans natural genetic diversity to identify novel mechanisms by which environmental toxins affect organismal physiology.
References
More filters
Journal ArticleDOI

Membrane lipids: where they are and how they behave.

TL;DR: How do cells apply anabolic and catabolic enzymes, translocases and transporters, plus the intrinsic physical phase behaviour of lipids and their interactions with membrane proteins, to create the unique compositions and multiple functions of their individual membranes?
Journal ArticleDOI

Prostaglandins and Leukotrienes: Advances in Eicosanoid Biology

TL;DR: Important insights into the mechanisms of inflammatory responses, pain, and fever have been gleaned from the current understanding of eicosanoid biology.
Journal ArticleDOI

A C. elegans mutant that lives twice as long as wild type

TL;DR: Finding that mutations in the gene daf-2 can cause fertile, active, adult Caenorhabditis elegans hermaphrodites to live more than twice as long as wild type raises the possibility that the longevity of the dauer is not simply a consequence of its arrested growth, but instead results from a regulated lifespan extension mechanism that can be uncoupled from other aspects of dauer formation.
Journal ArticleDOI

A specific amyloid-|[beta]| protein assembly in the brain impairs memory

TL;DR: It is found that memory deficits in middle-aged Tg2576 mice are caused by the extracellular accumulation of a 56-kDa soluble amyloid-β assembly, which is proposed to be Aβ*56 (Aβ star 56), which may contribute to cognitive deficits associated with Alzheimer's disease.
Related Papers (5)