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Investigating the Function and Evolutionary Context of WI12Rhg1 in Soybean Cyst Nematode Resistance
Investigating the Function and Evolutionary Context of WI12Rhg1 in Soybean Cyst Nematode R...
Investigating the Function and Evolutionary Context of WI12Rhg1 in Soybean Cyst Nematode Resistance

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자료유형  
 학위논문 서양
최종처리일시  
20260202105124
ISBN  
9798291547465
DDC  
581
저자명  
Lowenstein, Aaron.
서명/저자  
Investigating the Function and Evolutionary Context of WI12Rhg1 in Soybean Cyst Nematode Resistance
발행사항  
[Sl] : The University of Wisconsin - Madison, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
166 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-02, Section: B.
주기사항  
Advisor: Bent, Andrew.
학위논문주기  
Thesis (Ph.D.)--The University of Wisconsin - Madison, 2025.
초록/해제  
요약Soybean cyst nematode (SCN, Heterodera glycines) is the most economically damaging pathogen of soybean. Resistance to SCN in commercial soybean cultivars primarily depends on the Rhg1 locus, a multi-gene locus that encodes three proteins that contribute to SCN resistance. The least-characterized Rhg1-encoded protein is the wound-inducible domain-containing protein WI12Rhg1 encoded by Glyma.18G022700. WI12 proteins have no known function but have been implicated in reproductive development and responses to various biotic and abiotic stresses. This thesis research investigated the function and evolutionary context of WI12Rhg1 in SCN resistance. Silencing WI12Rhg1 in whole plants compromised resistance to both HG 0 and HG 2.5.7 SCN populations, demonstrating that WI12Rhg1 expression is necessary for full rhg1-b-mediated resistance. Transcriptomic and metabolomic experiments revealed that silencing WI12Rhg1 resulted in widespread transcriptional changes, dramatically reduced accumulation of salicylic acid, shifted the flux of phenylpropanoid metabolism away from downstream products, inhibited induction of defense signaling pathways, and caused dysregulation of gibberellic acid (GA) signaling. This work also clarified conflicting reports regarding the impact of GA on SCN resistance, as exogenous application of GA increased SCN resistance. RNA-seq data and RT-qPCR results revealed that WI12Rhg1 may impact DELLA stability as well as mir159 expression, which have been implicated in GA-mediated SCN resistance. Exploration of WI12Rhg1 gene structure revealed the presence of a non-canonical CUG translation start site upstream of the annotated ATG start site and found that this WI12 CUG and resulting N-terminal extension are highly conserved across land plant lineages. Analyses of WI12 gene structure, phylogeny, and M. truncatula Ribo-seq data provided multiple lines of evidence for translation initiation occurring at the CUG. Immunoblotting revealed that the observed WI12Rhg1 protein changes in different expression systems and that WI12Rhg1 forms high molecular weight complexes, potentially due to stable protein-protein interactions. Immunoblotting of myc-tagged WI12Rhg1 confirmed that translation from the CUG position can yield a stable protein in soybean and Nicotiana benthamiana, however endogenous use of the CUG start site remains unconfirmed. Together, these findings establish WI12Rhg1 as a broad modulator of plant defense, hormone signaling and metabolic balance, and suggest non-canonical translation initiation in the WI12 gene family. 
일반주제명  
Plant pathology
일반주제명  
Molecular biology
일반주제명  
Plant sciences
일반주제명  
Immunology
키워드  
Soybean cyst nematode
키워드  
WI12 proteins
키워드  
Gibberellic acid signaling
키워드  
Immunoblotting
키워드  
Nicotiana benthamiana
기타저자  
The University of Wisconsin - Madison Plant Pathology
기본자료저록  
Dissertations Abstracts International. 87-02B.
전자적 위치 및 접속  
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MARC

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■035    ▼a(MiAaPQ)AAI32238613
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a581
■1001  ▼aLowenstein,  Aaron.
■24510▼aInvestigating  the  Function  and  Evolutionary  Context  of  WI12Rhg1  in  Soybean  Cyst  Nematode  Resistance
■260    ▼a[Sl]▼bThe  University  of  Wisconsin  -  Madison▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a166  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-02,  Section:  B.
■500    ▼aAdvisor:  Bent,  Andrew.
■5021  ▼aThesis  (Ph.D.)--The  University  of  Wisconsin  -  Madison,  2025.
■520    ▼aSoybean  cyst  nematode  (SCN,  Heterodera  glycines)  is  the  most  economically  damaging  pathogen  of  soybean.  Resistance  to  SCN  in  commercial  soybean  cultivars  primarily  depends  on  the  Rhg1  locus,  a  multi-gene  locus  that  encodes  three  proteins  that  contribute  to  SCN  resistance.  The  least-characterized  Rhg1-encoded  protein  is  the  wound-inducible  domain-containing  protein  WI12Rhg1  encoded  by  Glyma.18G022700.  WI12  proteins  have  no  known  function  but  have  been  implicated  in  reproductive  development  and  responses  to  various  biotic  and  abiotic  stresses.  This  thesis  research  investigated  the  function  and  evolutionary  context  of  WI12Rhg1  in  SCN  resistance.  Silencing  WI12Rhg1  in  whole  plants  compromised  resistance  to  both  HG  0  and  HG  2.5.7  SCN  populations,  demonstrating  that  WI12Rhg1  expression  is  necessary  for  full  rhg1-b-mediated  resistance.  Transcriptomic  and  metabolomic  experiments  revealed  that  silencing  WI12Rhg1  resulted  in  widespread  transcriptional  changes,  dramatically  reduced  accumulation  of  salicylic  acid,  shifted  the  flux  of  phenylpropanoid  metabolism  away  from  downstream  products,  inhibited  induction  of  defense  signaling  pathways,  and  caused  dysregulation  of  gibberellic  acid  (GA)  signaling.  This  work  also  clarified  conflicting  reports  regarding  the  impact  of  GA  on  SCN  resistance,  as  exogenous  application  of  GA  increased  SCN  resistance.  RNA-seq  data  and  RT-qPCR  results  revealed  that  WI12Rhg1  may  impact  DELLA  stability  as  well  as  mir159  expression,  which  have  been  implicated  in  GA-mediated  SCN  resistance.  Exploration  of  WI12Rhg1  gene  structure  revealed  the  presence  of  a  non-canonical  CUG  translation  start  site  upstream  of  the  annotated  ATG  start  site  and  found  that  this  WI12  CUG  and  resulting  N-terminal  extension  are  highly  conserved  across  land  plant  lineages.  Analyses  of  WI12  gene  structure,  phylogeny,  and  M.  truncatula  Ribo-seq  data  provided  multiple  lines  of  evidence  for  translation  initiation  occurring  at  the  CUG.  Immunoblotting  revealed  that  the  observed  WI12Rhg1  protein  changes  in  different expression  systems  and  that  WI12Rhg1  forms  high  molecular  weight  complexes,  potentially  due  to  stable  protein-protein  interactions.  Immunoblotting  of  myc-tagged  WI12Rhg1  confirmed  that  translation  from  the  CUG  position  can  yield  a  stable  protein  in  soybean  and  Nicotiana  benthamiana,  however  endogenous  use  of  the  CUG  start  site  remains  unconfirmed.  Together,  these  findings  establish  WI12Rhg1  as  a  broad  modulator  of  plant  defense,  hormone  signaling  and  metabolic  balance,  and  suggest  non-canonical  translation  initiation  in  the  WI12  gene  family. 
■590    ▼aSchool  code:  0262.
■650  4▼aPlant  pathology
■650  4▼aMolecular  biology
■650  4▼aPlant  sciences
■650  4▼aImmunology
■653    ▼aSoybean  cyst  nematode
■653    ▼aWI12  proteins  
■653    ▼aGibberellic  acid  signaling
■653    ▼aImmunoblotting  
■653    ▼aNicotiana  benthamiana
■690    ▼a0480
■690    ▼a0307
■690    ▼a0479
■690    ▼a0982
■71020▼aThe  University  of  Wisconsin  -  Madison▼bPlant  Pathology.
■7730  ▼tDissertations  Abstracts  International▼g87-02B.
■790    ▼a0262
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17359474▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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