Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractFasciola hepatica: a light and electron microscope study of sustentacular tissue and heterophagy in the testis    Next AbstractKey enzymes involved in methionine catabolism by cheese lactic acid bacteria »

Dev Cell


Title:Methylation of the sterol nucleus by STRM-1 regulates dauer larva formation in Caenorhabditis elegans
Author(s):Hannich JT; Entchev EV; Mende F; Boytchev H; Martin R; Zagoriy V; Theumer G; Riezman I; Riezman H; Knolker HJ; Kurzchalia TV;
Address:"Max Planck Institute for Molecular Cell Biology and Genetics, Dresden, Germany"
Journal Title:Dev Cell
Year:2009
Volume:16
Issue:6
Page Number:833 - 843
DOI: 10.1016/j.devcel.2009.04.012
ISSN/ISBN:1878-1551 (Electronic) 1534-5807 (Linking)
Abstract:"In response to pheromone(s), Caenorhabditis elegans interrupts its reproductive life cycle and enters diapause as a stress-resistant dauer larva. This decision is governed by a complex system of neuronal and hormonal regulation. All the signals converge onto the nuclear hormone receptor DAF-12. A sterol-derived hormone, dafachronic acid (DA), supports reproductive development by binding to DAF-12 and inhibiting its dauer-promoting activity. Here, we identify a methyltransferase, STRM-1, that modulates DA levels and thus dauer formation. By modifying the substrates that are used for the synthesis of DA, STRM-1 can reduce the amount of hormone produced. Loss of STRM-1 function leads to elevated levels of DA and inefficient dauer formation. Sterol methylation was not previously recognized as a mechanism for regulating hormone activity. Moreover, the C-4 sterol nucleus methylation catalyzed by STRM-1 is unique to nematodes and thus could be a target for therapeutic strategies against parasitic nematode infections"
Keywords:Animals Caenorhabditis elegans/cytology/enzymology/*growth & development/*metabolism Caenorhabditis elegans Proteins/genetics/*metabolism Cholestenes/metabolism Cholesterol/metabolism Cytochrome P-450 Enzyme System/metabolism Gene Deletion Gene Expression;
Notes:"MedlineHannich, J Thomas Entchev, Eugeni V Mende, Fanny Boytchev, Hristio Martin, Rene Zagoriy, Vyacheslav Theumer, Gabriele Riezman, Isabelle Riezman, Howard Knolker, Hans-Joachim Kurzchalia, Teymuras V eng Research Support, Non-U.S. Gov't 2009/06/18 Dev Cell. 2009 Jun; 16(6):833-43. doi: 10.1016/j.devcel.2009.04.012"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-12-2024