STENOFOLIA Gene and Regulation of Somatic Embryogenesis
in Medicago truncatulа1
V. E. Tvorogovaa, *, Yu. A. Fedorovaa, F. Zhangb, and L. A. Lutovaa
Translated by M. Shulskaya
aDepartment of Genetics and Biotechnology, St. Petersburg State University, St. Petersburg, 199034 Russia
bOklahoma State University, Institute for Agricultural Biosciences, Department of Plant and Soil Sciences, Ardmore, Oklahoma, 73401 United States
Correspondence to: *e-mail: krubaza@mail.ru
1Abbreviations: RT-PCR—real-time PCR; SE—somatic embryogenesis; MtGEA—Medicago truncatula Gene Expression Atlas; STFoe—STF overexpression.
Received 18 January, 2016
Abstract—Expression of STENOFOLIA (STF) gene was analyzed in different organs of line R-108 barrel medic plants (Medicago truncatula Gaertn.). Maximum levels of STF expression were observed in the generative organs, fruits and flowers, suggesting its involvement in the reproduction process. The local analysis of STF expression during somatic embryogenesis in M. truncatula showed that the STF promoter is activated directly in somatic embryos. Overexpression of STF gene in the calli of R-108 line leads to increased embryogenicity, accompanied by reduced levels of MtGH3.6 gene expression, which is responsible for auxin metabolism, and also reduced expression levels of gene encoding MtHB1 transcription factor. Comparative analysis of MtGH3.6 and MtHB1 gene expression dynamics in the calli of embryogenic 2HA line and non-embryogenic A17 line of M. truncatula showed that these genes demonstrated reduced level of expression in embryogenic calli compared to non-embryogenic. These data suggested that STF stimulates the formation of somatic embryos, directly or indirectly inhibiting the transcription of MtGH3.6, MtHB1 and, probably, many other genes.
Keywords: Medicago truncatula, embryogenic and non-embryogenic calli, somatic embryogenesis, transcription factors, STENOFOLIA
DOI: 10.1134/S1021443716060133