• 제목/요약/키워드: Rlm1 gene

검색결과 3건 처리시간 0.014초

Detection of Blackleg Resistance Gene Rlm1 in Double-Low Rapeseed Accessions from Sichuan Province, by Kompetitive Allele-Specific PCR

  • Chai, Liang;Zhang, Jinfang;Dilantha Fernando, Wannakuwattewaduge Gerard;Li, Haojie;Huang, Xiaoqin;Cui, Cheng;Jiang, Jun;Zheng, Benchuan;Liu, Yong;Jiang, Liangcai
    • The Plant Pathology Journal
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    • 제37권2호
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    • pp.194-199
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    • 2021
  • Blackleg is a serious disease in Brassica plants, causing moderate to severe yield losses in rapeseed worldwide. Although China has not suffered from this disease yet (more aggressive Leptosphaeria maculans is not present yet), it is crucial to take provisions in breeding for disease resistance to have excellent blackleg-resistant cultivars already in the fields or in the breeding pipeline. The most efficient strategy for controlling this disease is breeding plants with identified resistance genes. We selected 135 rapeseed accessions in Sichuan, including 30 parental materials and 105 hybrids, and we determined their glucosinolate and erucic acid content and confirmed 17 double-low materials. A recently developed single-nucleotide polymorphism (SNP) marker, SNP_208, was used to genotype allelic Rlm1/rlm1 on chromosome A07, and 87 AvrLm1-resistant materials. Combined with the above-mentioned seed quality data, we identified 11 AvrLm1-resistant double-low rapeseed accessions, including nine parental materials and two hybrids. This study lays the foundation of specific R gene-oriented breeding, in the case that the aggressive Leptosphaeria maculans invades and establishes in China in the future and a robust and less labor consuming method to identify resistance in canola germplasm.

Role of MAPK Signaling Pathways in Regulating the Hydrophobin Cryparin in the Chestnut Blight Fungus Cryphonectria parasitica

  • So, Kum-Kang;Kim, Dae-Hyuk
    • Mycobiology
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    • 제45권4호
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    • pp.362-369
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    • 2017
  • We assessed the regulation of cryparin, a class II hydrophobin, using three representative mitogen-activated protein kinase (MAPK) pathways in Cryphonectria parasitica. Mutation of the CpSlt2 gene, an ortholog of yeast SLT2 in the cell wall integrity (CWI) pathway, resulted in a dramatic decrease in cryparin production. Similarly, a mutant of the CpBck1 gene, a MAP kinase kinase kinase gene in the CWI pathway, showed decreased cryparin production. Additionally, mutation of the cpmk1 gene, an ortholog of yeast HOG1, showed decreased cryparin production. However, mutation of the cpmk2 gene, an ortholog of yeast Kss1/Fus3, showed increased cryparin production. The easy-wet phenotype and accumulation of the cryparin transcript in corresponding mutants were consistent with the cryparin production results. In silico analysis of the promoter region of the cryparin gene revealed the presence of binding motifs related to downstream transcription factors of CWI, HOG1, and pheromone responsive pathways including MADS-box- and Ste12-binding domains. Real-time reverse transcriptase PCR analyses indicated that both CpRlm1, an ortholog of yeast RLM1 in the CWI pathway, and cpst12, an ortholog of yeast STE12 in the mating pathway, showed significantly reduced transcription levels in the mutant strains showing lower cryparin production in C. prasitica. However, the transcription of CpMcm1, an ortholog of yeast MCM1, did not correlate with that of the mutant strains showing downregulation of cryparin. These results indicate that three representative MAPK pathways played a role in regulating cryparin production. However, regulation varied depending on the MAPK pathways: the CWI and HOG1 pathways were stimulatory, whereas the pheromone-responsive MAPK was repressive.

Neurospora crassa ars-1 프로모터의 발현율 조사 (Transcription level of the ars-1 promoter of Neurospora crassa)

  • 이병욱;구상호
    • 생명과학회지
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    • 제13권2호
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    • pp.191-196
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    • 2003
  • Arylsulfatase를 암호화하는 Neurospora crassa의 ars-1 유전자는 황의 결핍에 의해서 발현이 조절된다. lacZ 유전자에 연결된 ars-1 프로모터 (Pars)가 N. crassa RLM 35-35 a his-3 inl 균주에 형질전환되고, 유사 서열 재조합에 의한 단일 교차에 의해서 염색체의 his-3 부위로 도입이 되었다. 황이 결여된 Vogel의 배지에서 자란 균사로부터 $\beta$-galactosidase 활성이 측정되었다. $\beta$-galactosidase 활성은 derepression 조건으로 변환한지 14 시간 후에 최고치를 기록하였다. Microconidiation에 의해서 생산된 homokaryon에서 측정된 활성은 heterokaryon보다 17% 증가가 되었음을 보여주었다. 이 실험은 ars-1 프로모터의 발현율을 측정할 수 있는 한 방법을 제시한 것으로, 보다 수월한 ars-1 발현 조절 연구가 기능할 것이다.