Document Type : Original Article

Authors

Department of Plant Sciences and Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran

Abstract

Introduction
Potato (Solanum tuberosum L.) is an economic crop that is grown and consumed worldwide. Potato is considered as the fourth important crop for human consumption after maize, wheat, and rice. Potato contain more carbohydrates, proteins, minerals, and vitamins per unit area than cereals. However, this crops exposed environmental stresses during growth and developmental stages particularly, drought stress. Potato is sensitive to drought condition because of narrow root system. As a result, it is necessary the investigation of molecular mechanism involved in drought stress in potato. Drought stress affected on the integrity and structure maintain of biological membrane. The actin-based myosin is necessary for the growth and organization of the endomembrane system. Given that myosin genes allow to move intercellular and intracellular providing the possibility of repair of damaged membrane areas under drought stress in plants. In eukaryotic cells, organelle movement, positioning and communications are critical for maintaining cellular functions and are highly regulated by intracellular trafficking. Directional movement of motor proteins along the cytoskeleton is one of the key regulators of such trafficking. Most plants have developed a unique actin–myosin system for intracellular trafficking. Myosins participate in a different cellular processes, endocytosis, containing cell polarization, intracellular and organellar transport, transcriptional regulation, and signal transduction. Motions are as molecular motors in biological systems. These can bind to filamentous actin and produce physical forces through hydrolyzing ATP. Myosins is one of the most diverse and largest protein families in eukaryote. Class XI and VIII motor proteins are characterized as a slow and fast motor proteins. Myosin XI possess many genes in Angiosperms. Whereas, myosin-VIII contain fewer members against class XI. Further, molecular size of myosin-VIII is smaller than myosin-XI.
Materials and methods
Protein file of A.thaliana was downloaded and matrix file of hidden Markov Model (HMM) of myosin gene family was used. Here, phylogenetic analysis, gene structure, and gene expression were surveyed. Gene expression of two genes (StMyoXI-F and StMyoXI-B) was performed in different tissues (root, stem, leaves, and tuber). For analysis of expression in different tissues (leaves, stem, and root), sampling was performed 2 weeks after mother tuber growth. However, tubers were sampled 6 weeks after cultivated in Karaj. To evaluate expression under drought stress, after 6 weeks of growth, the water stress was induced by irrigation suppression in 2 weeks while, daily irrigation was maintained for control plants. Leaves and tuber sampling were performed under two conditions.
Results and discussion
The seven StMyo genes were unevenly distributed in the two subgroups. The seven StMyo genes were unevenly distributed in the two subgroups. Class XI was the largest subfamily, which class VIII had the lowest subfamily. Drought treatment significantly increased expression of StMyoXI-B and StMyoXI-F genes by 80 and 8 fold compared to the control treatment, repectively. Under control conditions, StMyoXI-B and StMyoXI-F enhanced expression in root by 25 and 20 fold while, it showed low expression in leaves under control conditions. Under control conditions, StMyoXI-F gene showed the 3 and 4 fold change higher mean relative expression than the reference gene. The relative expression of StMyoXI-B gene has been increased 5 and 10 fold change in leaves and stem under non-stress conditions as compared to the reference gene. Among myosin genes, the number of exons varied from 1 to 39. Most of class-VIII proteins had fewer introns whereas, class-XI proteins possess more proteins than class VIII. This results indicated that occurred splicing process in the myosin genes.
Conclusion
Based on the obtained results, it is considered that these genes highly do not influenced in stem development. However, it had significantly affected in root, leaves, and tuber development. It seems this gene can be potentially a good candidate for drought tolerance breeding programs in potato.

Keywords

Main Subjects

Avisar, D., Prokhnevsky, A. I., Makarova, K. S., Koonin, E.V., Dolja, V.V., 2008. Myosin XI-K is required for rapid trafficking of Golgi stacks, peroxisomes, and mitochondria in leaf cells of Nicotiana benthamiana. Plant Physiology. 146, 1098-1108.
Camire, M.E., Kubow, S., Donnelly, D.J., 2009. Potatoes and human health. Critical Reviews in Food Science and Nutrition. 49, 823-840.
Foti, S., Mauromicale, G., Ierna, A., 1995. Influence of irrigation regimes on growth and yield of potato cv. Spunta. Potato research. 38, 307-317.
George, B.A., 2011. Stress effects on Myosin mutant root length in Arabidopsis thaliana. MSc dissertation, Faculty of University of Tennessee, Knoxville Knoxville, Tennessee, United States
Ghosh, D., Xu, J., 2014. Abiotic stress responses in plant roots: a proteomics perspective. Frontiers in Plant Science. 5, 1-13
Hajibarat, Z., Saidi, A., Hajibarat, Z., 2018. Bioinformatics analysis of MADS-box in Brachypodium distachyon. Crop Biotechnology. 8, 1-15. [In Persian with Wnglish summary].
Hajibarat, Z., Saidi, A., Zeinalabedini, M., Gorji, A.M., Ghaffari, M.R., Shariati, V., Ahmadvand, R., 2022. Genome-wide identification of StU-box gene family and assessment of their expression in developmental stages of Solanum tuberosum. Journal of Genetic Engineering and Biotechnology. 20, 1-21.
Haraguchi, T., Ito, K., Duan, Z., Rula, S., Takahashi, K., Shibuya, Y., Hagino, N., Miyatake, Y., Nakano, A., Tominaga, M., 2018. Functional diversity of class XI myosins in Arabidopsis thaliana. Plant and Cell Physiology. 59, 2268-2277.
Haraguchi, T., Tamanaha, M., Suzuki, K., Yoshimura, K., Imi, T., Tominaga, M., Sakayama, H., Nishiyama, T., Murata, T., Ito, K., 2022. Discovery of ultrafast myosin, its amino acid sequence, and structural features. Proceedings of the National Academy of Sciences. 119, 2120962119.
Haraguchi, T., Tominaga, M., Matsumoto, R., Sato, K., Nakano, A., Yamamoto, K., Ito, K., 2014. Molecular characterization and subcellular localization of Arabidopsis class VIII Myosin, ATM1. Journal of Biological Chemistry. 289, 12343-12355.
Hasanpanah, D., Nikshad, k., Hasani, M., Aghazadeh, B., 2003. Potato in Ardabil Province, Ardabil Agriculture Jihad Organization. 64p. [In Persian].
Jiang, S., Ramachandran, S., 2004. Identification and molecular characterization of myosin gene family in Oryza sativa genome. Plant and Cell Physiology. 45, 590-599.
Lee, Y.R.J., Liu, B., 2004. Cytoskeletal motors in Arabidopsis: sixty-one kinesins and seventeen myosins. Plant Physiology. 136, 3877–3883.
Li, F., Fan, G., Lu, C., Xiao, G., Zou, C., Kohel, R.J., Ma, Z., Shang, H., Ma, X., Wu, J., Liang, X., 2015. Genome sequence of cultivated Upland cotton (Gossypium hirsutum TM-1) provides insights into genome evolution. Nature Biotechnology. 33, 524-530.
Livak, K.J., Schmittgen, T.D., 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods. 25, 402-408.
Ma, C., Zhao, Z., Wang, N., Azhar, M.T., Du, X., 2020. Genome-wide identification and comparative analysis of myosin gene family in four major cotton species. Genes. 11. 731.
Mane, S.P., Robinet, C.V., Ulanov, A., Schafleitner, R., Tincopa, L., Gaudin, A., Nomberto, G., Alvarado, C., Solis, C., Bolivar, L.A., Blas, R., 2008. Molecular and physiological adaptation to prolonged drought stress in the leaves of two Andean potato genotypes. Functional Plant Biology. 35, 669-688.
Natesan, S.K.A., Sullivan, J.A. and Gray, J.C., 2009. Myosin XI is required for actinassociated movement of plastid stromules. Molecular Plant. 2, 1262–1272.
Nebenführ, A., Dixit, R., 2018. Kinesins and myosins: molecular motors that coordinate cellular functions in plants. Annual Review of Plant Biology. 69, 329-361.
Ojangu, E.L., Järve, K., Paves, H. and Truve, E.,  2007. Arabidopsis thaliana myosin XIK is involved in root hair as well as trichome morphogenesis on stems and leaves. Protoplasma. 230, 193–202
Peremyslov, V.V., Prokhnevsky, A.I., Dolja, V.V., 2010. Class XI myosins are required for development, cell expansion, and F-actin organization in Arabidopsis. Plant Cell. 22, 1883–1897
Peremyslov, V.V., Cole, R.A., Fowler, J.E., Dolja, V.V., 2015. Myosin-powered membrane compartment drives cytoplasmic streaming, cell expansion and plant development. PloS One. 10, 1-19.
Peremyslov, V.V., Prokhnevsky, A.I., Dolja, V.V., 2010. Class XI myosins are required for development, cell expansion, and F-Actin organization in Arabidopsis. The Plant Cell. 22, 1883-1897.
Peremyslov, V.V., Mockler, T.C., Filichkin, S.A., Fox, S.E., Jaiswal, P., Makarova, K.S., Koonin, E.V. and Dolja, V.V., 2011. Expression, splicing, and evolution of the myosin gene family in plants. Plant Physiology. 155, 1191-1204.
Peremyslov, V.V., Prokhnevsky, A.I., Avisar, D., Dolja, V.V., 2008a. Two class XI myosins function in organelle trafficking and root hair development in Arabidopsis. Plant Physiology. 146, 1109-1116.
Prokhnevsky, A.I., Peremyslov, V.V., Dolja, V.V., 2008. Overlapping functions of the four class XI myosins in Arabidopsis growth, root hair elongation, and organelle motility. Proceedings of the National Academy of Sciences. 105, 19744-19749.
Reddy, A.S., Day, I.S., 2001. Analysis of the myosins encoded in the recently completed Arabidopsis thaliana genome sequence. Genome Biology. 2, 1-19.
Saidi, A., Hajibarat, Z., 2020. In-silico analysis of eukaryotic translation initiation factors (eIFs) in response to environmental stresses in rice (Oryza sativa). Biologia. 75, 731-1738.
Sattarzadeh, A., Krahmer, J., Germain, A.D., Hanson, M.R., 2009. A myosin XI tail domain homologous to the yeast myosin vacuole-binding domain interacts with plastids and stromules in Nicotiana benthamiana. Molecular Plant. 2, 1351-1358.
Shimmen, T., Yokota, E., 2004. Cytoplasmic streaming in plants. Current Opinion in Cell Biology. 16, 68-72.
Sparkes, I.A., Teanby, N.A., Hawes, C., 2008. Truncated myosin XI tail fusions inhibit peroxisome, golgi, and mitochondrial movement in tobacco leaf epidermal cells: a genetic tool for the next generation. Journal of Experimental Botnay. 59, 2499–2512
Sparkes, I.A., 2010. Motoring around the plant cell: insights from plant myosins. Biochemical Society Transactions. 38, 833-838.
Syamaladevi, D.P., Spudich, J.A., Sowdhamini, R., 2012. Structural and functional insights on the Myosin superfamily. Bioinformatics and biology insights, 6. S8451.
Tingler, M., Kurz, S., Maerker, M., Ott, T., Fuhl, F., Schweickert, A., LeBlanc-Straceski, J.M., Noselli, S., Blum, M., 2018. A conserved role of the unconventional myosin 1d in laterality determination. Current Biology. 28, 810-816.
Titus, M.A., 2018. Myosin-driven intracellular transport.  Harbor Laboratory Press. Minnesota pp.10. https://dx.doi.org/0.1101/cshperspect.a021972
Ueda, H., Yokota, E., Kutsuna, N., Shimada, T., Tamura, K., Shimmen, T., Hasezawa, S., Dolja, V.V., Hara-Nishimura, I., 2010. Myosin-dependent endoplasmic reticulum motility and F-actin organization in plant cells. Proceedings of the National Academy of Sciences. 107, 6894-6899.
Vidali, L., Burkart, G.M., Augustine, R.C., Kerdavid, E., Tüzel, E., Bezanilla, M., 2010. Myosin XI is essential for tip growth in Physcomitrella patens. The Plant Cell. 22, 1868-1882.
Wang, G., Zhong, M., Wang, J., Zhang, J., Tang, Y., Wang, G., Song, R., 2014. Genome-wide identification, splicing, and expression analysis of the myosin gene family in maize (Zea mays). Journal of experimental botany. 65, 923-938.
Wu, S.Z., Ritchie, J.A., Pan, A.H., Quatrano, R.S., Bezanilla, M., 2011. Myosin VIII regulates protonemal patterning and developmental timing in the moss Physcomitrella patens. Molecular Plant. 4, 909-921.