Silencing of a meristematic gene using geminivirus‐derived vectors

• Published in: The Plant journal : for cell and molecular biology 2001-08, Vol.27 (4), p.357-366
• Main Authors: Peele, Charles, Jordan, Chad V., Muangsan, Nooduan, Turnage, Michael, Egelkrout, Erin, Eagle, Patricia, Hanley‐Bowdoin, Linda, Robertson, Dominique
• Format: Article
• Language: English
• Subjects: Base Sequence; Biological and medical sciences; DNA Primers; DNA, Viral - metabolism; functional genomics; Fundamental and applied biological sciences. Psychology; Geminiviridae - genetics; Geminiviruses; Gene expression; Gene Silencing; Genes, Essential; Genetic Vectors; homology‐dependent gene silencing; In Situ Hybridization; magnesium chelatase; meristem; Meristem - genetics; meristems; Molecular and cellular biology; Molecular genetics; Nicotiana - genetics; Nicotiana - virology; Nicotiana benthamiana; plant DNA viruses; proliferating cell nuclear antigen
• ISSN: 0960-7412; 1365-313X
• DOI: 10.1046/j.1365-313x.2001.01080.x

Summary Geminiviruses are DNA viruses that replicate and transcribe their genes in plant nuclei. They are ideal vectors for understanding plant gene function because of their ability to cause systemic silencing in new growth and ease of inoculation. We previously demonstrated DNA episome‐mediated gene silencing from a bipartite geminivirus in Nicotiana benthamiana. Using an improved vector, we now show that extensive silencing of endogenous genes can be obtained using less than 100 bp of homologous sequence. Concomitant symptom development varied depending upon the target gene and insert size, with larger inserts producing milder symptoms. In situ hybridization of silenced tissue in attenuated infections demonstrated that silencing occurs in cells that lack detectable levels of viral DNA. A mutation confining the virus to vascular tissue produced extensive silencing in mesophyll tissue, further demonstrating that endogenous gene silencing can be separated from viral infection. We also show that two essential genes encoding a subunit of magnesium chelatase and proliferating cell nuclear antigen (PCNA) can be silenced simultaneously from different components of the same viral vector. Immunolocalization of silenced tissue showed that the PCNA protein was down‐regulated throughout meristematic tissues. Our results demonstrate that geminivirus‐derived vectors can be used to study genes involved in meristem function in intact plants.