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Strain-Dependent Temperature-Sensitive Phase in Crown Gall Tumorigenesis
Author(s) -
Charles E. Rogler
Publication year - 1981
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.68.1.5
Subject(s) - gall , strain (injury) , crown (dentistry) , biology , carcinogenesis , phase (matter) , botany , chemistry , genetics , anatomy , materials science , composite material , gene , organic chemistry
The effect of high temperature treatments on the early stages of crown gall tumorigenesis in sunflowers was investigated. Treatments of 32 C initiated at various times during the first ten days after infection had a similar effect on tumors induced by Agrobacterium tumefaciens strains B(6) and C58. Tumor growth was sensitive to 32 C until 60 to 72 hours after infection and was stimulated by 32 C after that time. Therefore, the "inception phase" for both C58 and B(6)-induced tumors ends between 60 to 72 hours after infection. In contrast, B(6) and C58 tumors varied in their response to 37 C treatments during the first 168 hours after infection. Both C58 and B(6) tumors were sensitive to 37 C during the first 72 hours; however, B(6) tumors became resistant to 37 C after 96 hours, whereas C58-induced tumors remained sensitive until 144 to 168 hours after infection.The growth rate of C58 and B(6) tumors in plants moved to 32 C at 90 hours after infection was the same. B(6) tumors in plants moved to 37 C at 90 hours after infection also continued to grow rapidly, whereas C58 tumors in plants moved to 37 C at 90 hours exhibited a complete cessation of tumor growth. The 37 C temperature-sensitive period specific to C58 tumors ceases by 168 hours after infection. This indicates that the temperature-sensitive functions are no longer required after 168 hours. The possible significance of this work with regard to the presence of a temperature-sensitive plasmid, pTiC58, in strain C58 and the mechanism of tumor-inducing plasmid DNA maintenance in incipient tumor cells is discussed.

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