Expression Profiling of MAP Kinase–Mediated Meiotic Progression in Caenorhabditis elegans 英文参考文献.docVIP
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Expression Profiling of MAP Kinase–Mediated Meiotic Progression in Caenorhabditis elegans 英文参考文献
ExpressionProfilingofMAPKinase–
MediatedMeioticProgression
inCaenorhabditiselegans
Stefanie W. Leacock, Valerie Reinke*
DepartmentofGenetics,YaleUniversitySchoolofMedicine,NewHaven,Connecticut,UnitedStatesofAmerica
TheLET-60(Ras)/LIN-45(Raf)/MPK-1(MAPkinase)signalingpathwayplaysakeyroleinthedevelopmentofmultiple
tissuesinCaenorhabditiselegans.Forthemostpart,theidentitiesofthedownstreamgenesthatactastheultimate
effectors of MPK-1 signaling have remained elusive. A unique allele of mpk-1, ga111, displays a reversible,
temperature-sensitive, tissue-specific defect in progression through meiotic prophase I. We performed gene
expression profiling on mpk-1(ga111)animals toidentify candidate downstream effectorsof MPK-1signaling in the
germline.ThisanalysisdelineatedacohortofgeneswhoseexpressionrequiresMPK-1signalingingermcellsinthe
pachytenestageofmeiosisI.RNAinsituhybridizationanalysisshowsthatthesegenesareexpressedinthegermline
inanMPK-1-dependentmannerandhaveaspatialexpressionpatternconsistentwiththelocationofactivatedMPK-1.
We found that one MPK-1 signaling-responsive gene encoding a C2H2 zinc finger protein plays a role in meiotic
chromosome segregation downstream of MPK-1. Additionally, discovery of genes responsive to MPK-1 signaling
permittedustoorderMPK-1signalingrelativetoseveraleventsoccurringinpachytene,includingEFL-1/DPL-1gene
regulation and X chromosome reactivation. This study highlights the utility of applying global gene expression
methodstoinvestigategenesdownstreamofcommonlyusedsignalingpathwaysinvivo.
Citation: Leacock SW, ReinkeV (2006) Expression profiling of MAP kinase–mediated meiotic progression in Caenorhabditis elegans. PLoS Genet 2(11): e174. doi:10.1371/
journal.pgen.0020174
protein required for proper meiotic progression and oo-
genesis, is also present during pachytene and prevents
Introduction
Signal transduction pathways play key roles in specifying
cell fates. Most signaling pathways terminate in the nucleus
andaltertheexpressionofas
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