Plant DNA viruses and gene silencing

2000 ◽  
pp. 187-202
Author(s):  
Simon N. Covey ◽  
Nadia S. Al-Kaff
Keyword(s):  
2020 ◽  
Vol 117 (29) ◽  
pp. 16928-16937 ◽  
Author(s):  
Ya-Zhou He ◽  
Yu-Meng Wang ◽  
Tian-Yan Yin ◽  
Elvira Fiallo-Olivé ◽  
Yin-Quan Liu ◽  
...  

Whereas most of the arthropod-borne animal viruses replicate in their vectors, this is less common for plant viruses. So far, only some plant RNA viruses have been demonstrated to replicate in insect vectors and plant hosts. How plant viruses evolved to replicate in the animal kingdom remains largely unknown. Geminiviruses comprise a large family of plant-infecting, single-stranded DNA viruses that cause serious crop losses worldwide. Here, we report evidence and insight into the replication of the geminivirus tomato yellow leaf curl virus (TYLCV) in the whitefly (Bemisia tabaci) vector and that replication is mainly in the salivary glands. We found that TYLCV induces DNA synthesis machinery, proliferating cell nuclear antigen (PCNA) and DNA polymerase δ (Polδ), to establish a replication-competent environment in whiteflies. TYLCV replication-associated protein (Rep) interacts with whitefly PCNA, which recruits DNA Polδ for virus replication. In contrast, another geminivirus, papaya leaf curl China virus (PaLCuCNV), does not replicate in the whitefly vector. PaLCuCNV does not induce DNA-synthesis machinery, and the Rep does not interact with whitefly PCNA. Our findings reveal important mechanisms by which a plant DNA virus replicates across the kingdom barrier in an insect and may help to explain the global spread of this devastating pathogen.


2013 ◽  
Vol 199 (2) ◽  
pp. 464-475 ◽  
Author(s):  
Edgar Rodríguez-Negrete ◽  
Rosa Lozano-Durán ◽  
Alvaro Piedra-Aguilera ◽  
Lucia Cruzado ◽  
Eduardo R. Bejarano ◽  
...  

1985 ◽  
Vol 2 (4) ◽  
pp. 287-316 ◽  
Author(s):  
Stephen H. Howell ◽  
Robert M. Goodman

2021 ◽  
Vol 12 ◽  
Author(s):  
Karuppannan Veluthambi ◽  
Sukumaran Sunitha

Geminiviruses are plant DNA viruses that infect a wide range of plant species and cause significant losses to economically important food and fiber crops. The single-stranded geminiviral genome encodes a small number of proteins which act in an orchestrated manner to infect the host. The fewer proteins encoded by the virus are multifunctional, a mechanism uniquely evolved by the viruses to balance the genome-constraint. The host-mediated resistance against incoming virus includes post-transcriptional gene silencing, transcriptional gene silencing, and expression of defense responsive genes and other cellular regulatory genes. The pathogenicity property of a geminiviral protein is linked to its ability to suppress the host-mediated defense mechanism. This review discusses what is currently known about the targets and mechanism of the viral suppressor AC2/AL2/transcriptional activator protein (TrAP) and explore the biotechnological applications of AC2.


2006 ◽  
Vol 80 (11) ◽  
pp. 5405-5412 ◽  
Author(s):  
Takashi Mino ◽  
Takeaki Hatono ◽  
Naoki Matsumoto ◽  
Tomoaki Mori ◽  
Yusuke Mineta ◽  
...  

ABSTRACT Recently, we demonstrated that plant DNA virus replication was inhibited in planta by using an artificial zinc finger protein (AZP) and created AZP-based transgenic plants resistant to DNA virus infection. Here we apply the AZP technology to the inhibition of replication of a mammalian DNA virus, human papillomavirus type 18 (HPV-18). Two AZPs, designated AZPHPV-1 and AZPHPV-2, were designed by using our nondegenerate recognition code table and were constructed to block binding of the HPV-18 E2 replication protein to the replication origin. Both of the newly designed AZPs had much higher affinities towards the replication origin than did the E2 protein, and they efficiently blocked E2 binding in vitro. In transient replication assays, both AZPs inhibited viral DNA replication, especially AZPHPV-2, which reduced the replication level to approximately 10%. We also demonstrated in transient replication assays, using plasmids with mutant replication origins, that AZPHPV-2 could precisely recognize the replication origin in mammalian cells. Thus, it was demonstrated that the AZP technology could be applied not only to plant DNA viruses but also to mammalian DNA viruses.


1998 ◽  
Vol 14 (1) ◽  
pp. 91-100 ◽  
Author(s):  
Susanne Kjemtrup ◽  
Kim S. Sampson ◽  
Charles G. Peele ◽  
Long V. Nguyen ◽  
Mark A. Conkling ◽  
...  
Keyword(s):  

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