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  Two independent sulfation processes regulate mouth-form plasticity in the nematode Pristionchus pacificus

Namdeo, S., Moreno, E., Rödelsperger, C., Baskaran, P., Witte, H., & Sommer, R. (2018). Two independent sulfation processes regulate mouth-form plasticity in the nematode Pristionchus pacificus. Development, 145(13): dev166272. doi:10.1242/dev.166272.

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 Creators:
Namdeo, S1, Author           
Moreno, E1, Author           
Rödelsperger, C1, Author           
Baskaran, P1, Author           
Witte, H1, Author           
Sommer, RJ1, Author           
Affiliations:
1Department Integrative Evolutionary Biology, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3375786              

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Free keywords: Animals Helminth Proteins/*metabolism Mouth/cytology/*embryology Nematoda/cytology/*embryology *Developmental plasticity *Developmental switch gene *Eud-1/sulfatase *Pristionchus pacificus *Sulfotransferases
 Abstract: Sulfation of biomolecules, like phosphorylation, is one of the most fundamental and ubiquitous biochemical modifications with important functions during detoxification. This process is reversible, involving two enzyme classes: a sulfotransferase, which adds a sulfo group to a substrate; and a sulfatase that removes the sulfo group. However, unlike phosphorylation, the role of sulfation in organismal development is poorly understood. In this study, we find that two independent sulfation events regulate the development of mouth morphology in the nematode Pristionchus pacificus. This nematode has the ability to form two alternative mouth morphologies depending on environmental cues, an example of phenotypic plasticity. We found that, in addition to a previously described sulfatase, a sulfotransferase is involved in regulating the mouth-form dimorphism in P. pacificus However, it is unlikely that both of these sulfation-associated enzymes act upon the same substrates, as they are expressed in different cell types. Furthermore, animals mutant in genes encoding both enzymes show condition-dependent epistatic interactions. Thus, our study highlights the role of sulfation-associated enzymes in phenotypic plasticity of mouth structures in Pristionchus.

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 Dates: 2018-07
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1242/dev.166272
PMID: 29967123
 Degree: -

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Title: Development
  Other : Development
Source Genre: Journal
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Publ. Info: Cambridge, Cambridgeshire : Company of Biologists
Pages: 12 Volume / Issue: 145 (13) Sequence Number: dev166272 Start / End Page: - Identifier: ISSN: 0950-1991
CoNE: https://pure.mpg.de/cone/journals/resource/954927546241