Conserved mechanism of Wnt signaling function in the specification of vulval precursor fates in C. elegans and C. briggsae

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F10%3A00352047" target="_blank" >RIV/60077344:_____/10:00352047 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Conserved mechanism of Wnt signaling function in the specification of vulval precursor fates in C. elegans and C. briggsae

Popis výsledku v původním jazyce

To understand the function and evolution of Wnt signaling in Caenorhabditis nematodes we focused on C. briggsae, a species that is substantially divergent from C. elegans in terms of the evolutionary time scale yet shares almost identical morphology. Weisolated mutants in C briggsae that display multiple pseudo-vulvae resulting from ectopic VPC induction. We cloned one of these loci and found that it encodes an Axin homolog, Cbr-PRY-1. Our genetic studies revealed that Cbr-pry-1 functions upstream of the canonical Wnt pathway components Cbr-bar-1 (beta-catenin) and Cbr-pop-1(tcf/lef) as well as the Hox target Cbr-lin-39 (Dfd/Scr). We further characterized the pry-1 vulval phenotype in C briggsae and C elegans using 8 cell fate markers, cell ablation,and genetic interaction approaches. Our results show that ectopically induced VPCs in pry-1 mutants adopt 2 degrees fates independently of the gonad-derived inductive and LIN-12/Notch-mediated lateral signaling pathways.

Název v anglickém jazyce

Conserved mechanism of Wnt signaling function in the specification of vulval precursor fates in C. elegans and C. briggsae

Popis výsledku anglicky

To understand the function and evolution of Wnt signaling in Caenorhabditis nematodes we focused on C. briggsae, a species that is substantially divergent from C. elegans in terms of the evolutionary time scale yet shares almost identical morphology. Weisolated mutants in C briggsae that display multiple pseudo-vulvae resulting from ectopic VPC induction. We cloned one of these loci and found that it encodes an Axin homolog, Cbr-PRY-1. Our genetic studies revealed that Cbr-pry-1 functions upstream of the canonical Wnt pathway components Cbr-bar-1 (beta-catenin) and Cbr-pop-1(tcf/lef) as well as the Hox target Cbr-lin-39 (Dfd/Scr). We further characterized the pry-1 vulval phenotype in C briggsae and C elegans using 8 cell fate markers, cell ablation,and genetic interaction approaches. Our results show that ectopically induced VPCs in pry-1 mutants adopt 2 degrees fates independently of the gonad-derived inductive and LIN-12/Notch-mediated lateral signaling pathways.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

EB - Genetika a molekulární biologie

OECD FORD obor

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Projekt

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Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2010

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Developmental Biology

ISSN

0012-1606

e-ISSN

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Svazek periodika

346

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

12

Strana od-do

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Kód UT WoS článku

000281930900011

EID výsledku v databázi Scopus

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