Journal of Food and Nutrition Research
ISSN (Print): 2333-1119 ISSN (Online): 2333-1240 Website: https://www.sciepub.com/journal/jfnr Editor-in-chief: Prabhat Kumar Mandal
Open Access
Journal Browser
Go
Journal of Food and Nutrition Research. 2023, 11(1), 46-56
DOI: 10.12691/jfnr-11-1-5
Open AccessArticle

Sweet Sorghum (Sorghum bicolor L.) Cloning and Functional Analysis of Callose Gene SbGlu1 in Protein Content

Shen Hui Yong1, Hafeez Noor1, Dang Dexuan1, Gao Haiyan1, Liu Peng1, Zhang Yuan qing1 and Cheng Qingjun1,

1Shanxi Key Laboratory of Sorghum Genetic and Germplasm Innovation

Pub. Date: January 10, 2023

Cite this paper:
Shen Hui Yong, Hafeez Noor, Dang Dexuan, Gao Haiyan, Liu Peng, Zhang Yuan qing and Cheng Qingjun. Sweet Sorghum (Sorghum bicolor L.) Cloning and Functional Analysis of Callose Gene SbGlu1 in Protein Content. Journal of Food and Nutrition Research. 2023; 11(1):46-56. doi: 10.12691/jfnr-11-1-5

Abstract

The Sweet sorghum (Sorghum bicolor L.) Moench is a variant of grain sorghum, which origins in Africa. Due to its high sugar and tolerance, it has been considered as a potentially useful energy crop and received more attention. However, less study on sweet sorghum has been performed in physiology and molecular by Al stress. These results illustrated that the decrease of β-1,3-glucanase activity by Al could lead to callose accumulation. In POTCHETSTRM, five β-1,3-glucanase genes expression were up-regulated, and a gene expression was down-regulated. In ROMA, only one β-1,3-glucanase gene, SbGlu1 (Sb03g045630.1) expressed response to Al, and the expression was higher in ROMA than in POTCHETSTRM. The expression levels of six callose synthase-like genes were very low exposure of 10 µM Al upon to 24 h in ROMA, but POTCHETSTRM exhibited the highest expression level only at 24 h. Therefore, callose synthase-like genes maybe regulate callose deposition in the later stage of Al stress in sweet sorghum. The SbGlu1 expression positively correlated with callose content in both cultivars. The SbGlu1 expression maybe involve in callose degradation in sweet sorghum by Al stress. The full-length cDNAs of SbGlu1 were cloned from the root tips of both ROMA and POTCHETSTRM, respectively. The SbGlu1 were transient expressed in onion epidermal cells for subcellular localization, showed that SbGLU1 is soluble with no specificity localization.

Keywords:
sweet sorghum Callose β-1,3-glucanase gene different expressed gene protein content

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Figures

Figure of 7

References:

[1]  Horst W., Püschel A. K. and Schmohl N. Induction of callose formation is a sensitive marker for genotypic aluminium sensitivity in maize. Plant and Soil, 192:23-30, 1997.
 
[2]  Jones D.L. and Kochian L.V. Aluminum Inhibition of the Inositol 1, 4, 5-Trisphosphate signal transduction pathway in wheat roots: a role in aluminum toxicity. Plant Cell7:1913-1922, 1995.
 
[3]  Li Y. Y., Yang J. L., Zhang Y. J. and Zheng S. J. Disorganized distribution of homogalacturonan epitopes in cell walls as one possible mechanism for aluminium-induced root growth inhibition in maize. Annals of Botany.104: 235-241, 2009.
 
[4]  Zhou Shaoqun, Lou Yann-Ru, Tzin Vered, Jander Georg. Alteration of plant primary metabolism in response to insect herbivory. Plant Physiology, 169:1488-1498, 2015.
 
[5]  Rossi Magdalena, Goggin Fiona L, Milligan Stephen B, Kaloshian Isgouhi, Ullman Diane E, Williamson Valerie M. The nematode resistance gene Mi of tomato confers resistance against the potato aphid. Proceedings of the National Academy of Sciences of the United States of America, 95:9750-9754, 1998.
 
[6]  Tetreault Hannah M, Grover Sajjan, Scully Erin D, Gries Tammy, Palmer Nathan A, Sarath Gautam, Louis Joe, Sattler Scoot E. Global responses of resistant and susceptible sorghum (Sorghum bicolor) to Sugarcane Aphid (Melanaphis sacchari). Frontiers in Plant Science, 10:145, 2019.
 
[7]  Zhang Hengyou, Huang Jian, Huang Yinghua. Identification and characterization of plant resistance genes (R genes) in sorghum and their involvement in plant defense against aphids. Plant growth regulation, 96:443-461, 2022.
 
[8]  Kim D, Langmead B, Salzberg SL. HISAT: a fast spliced aligner with low memort requirements. Nature methods, 12 (4): 357-360, 2015.
 
[9]  Pertea M, Pertea G M, Antonescu C M, et al. StringTie enables improved reconstruction of a transcriptome from RNA-seq reads. Nature biotechnology, 33(3):290-295, 2015.
 
[10]  Kerchev PI, Fenton B, Foyer CH, Hancock RD. Plant responses to insect herbivory: interactions between photosynthesis, reactive oxygen species and hormonal signalling pathways. Plant Cell and Environment, 35: 441-453, 2012.
 
[11]  Donze-Reiner Teresa, Palmer Nathan A, Scully Erin D, Prochaska Travis J, Koch Kyle G, Heng-Moss Tiffany, Bradshaw Jeffrey D, Twigg Paul, Amundsen Keenan, Sattler Scott E, Sarath Gautam. Transcriptional analysis of defense mechanisms in upland tetraploid switchgrass to greenbugs. BMC Plant Biology, 17: 46, 2017.
 
[12]  Gutsche A, Heng-Moss T, Sarath G, Twigg P, Xia Y, Lu G, Mornihinweg D. Gene expression profiling of tolerant barley in response to Diuraphis noxia (Hemiptera: Aphididae) feeding. Bulletin of Entomological Research, 99: 163-173, 2009.
 
[13]  Prochaska TJ, Donze-Reiner T, Marchi-Werle L, Palmer NA, Hunt TE, Sarath G, Heng-Moss T Transcriptional responses of tolerant and susceptible soybeans to soybean aphid (Aphis glycines Matsumura) herbivory. Arthropod Plant Interactions, 9: 347-359, 2015.
 
[14]  Kiani Mahnaz, Szczepaniec Adrianna. Effects of sugarcane aphid herbivory on transcriptional responses of resistant and susceptible sorghum. BMC Genomics, 19:774, 2018.
 
[15]  Rahbe Yvan, Sauvion Nicolas, Febvay Gerard, Peumans Willy J, Gatehouse Angharad MR. Toxicity of lectins and processing of ingested proteins in the pea aphid Acyrthosiphon pisum. Entomologia Experimentalis Applicata, 76: 143-155, 1995.
 
[16]  Rogers Lindsay D, Overall Christopher M. Proteolytic post-translational modification of proteins: Proteomic tools and methodology. Molecular & cellular proteomics:MCP, 12: 3532-3542, 2013.
 
[17]  Smith C. Michael, Boyko Elena V. The molecular bases of plant resistance and defense responses to aphid feeding: current status. Entomologia Experimentalis Applicata, 122: 1-16, 2007.
 
[18]  Studham ME, and Macintosh GC. Multiple phytohormone signals control the transcriptional response to soybean aphid infestation in susceptible and resistant soybean plants. Molecular Plant-Microbe Interactions, 26: 116-129, 2013.
 
[19]  Kumar Shrestha, Huang Yinghua. Genome-wide characterization of the sorghum JAZ gene family and their responses to phytohormone treatments and aphid infestation. Scientific reports, 12: 3238, 2022.
 
[20]  Pan WB. Advances in the investigation of vegetable tannin and its effect on forage quality I. the character and function of vegetable tannins. Journal of Zhangzhou Technical institute, 10 (3): 58-61, 2008.
 
[21]  Dogramaci Mahmut, Mayo ZB, Wright Robert J, Reese John. Categories of resistance, antibiosis and tolerance to biotype I greenbug (Schizaphis graminum (Rondani) Homoptera Aphidiae) in four sorghum (Sorghum bicolor L.) Moench Poales: Gramineae) hybrids. Journal of the Kansas Entomological Society, 80: 183-191, 2007.
 
[22]  Ryan P.R., Raman H., Gupta S., Sasaki T., Yamamoto Y. and Delhaize E. The multiple origins of aluminium resistance in hexaploid wheat include Aegilops tauschii and more recent cis mutations to TaALMT1. Plant Journal, 64: 446-455, 2010.
 
[23]  Sasaki T., Ryan P.R., Delhaize E., Hebb D.M., Ogihara Y., Kawaura K., Noda K., Kojima T., Toyoda A. and Matsumoto H. Sequence upstream of the wheat (Triticum aestivum L.) ALMT1 gene and its relationship to aluminum resistance. Plant and Cell Physiology, 47: 1343-1354, 2006.
 
[24]  Liu J., Pineros M.A. and Kochian L.V. The role of aluminum sensing and signaling in plant aluminum resistance. Journal of Integrative Plant Biology, 56:221-230, 2014.
 
[25]  Tian Q.Y., Sun D.H., Zhao M.G. and Zhang W.H. Inhibition of nitric oxide synthase (NOS) underlies aluminum-induced inhibition of root elongation in Hibiscus moscheutos. New Phytologist, 174:322-331, 2007.
 
[26]  Toller A., Brownfield L., Neu C., Twell D. and Schulze-Lefert P. Dual function of Arabidopsis glucan synthase-like genes GSL8 and GSL10 in male gametophyte development and plant growth. Plant Journal, 54:911-923, 2008.
 
[27]  Wang H.H., Huang J.J. and Bi Y.R. Nitrate reductase-dependent nitric oxide production is involved in aluminum tolerance in red kidney bean roots. Plant Science, 179, 281-288, 2010.
 
[28]  Liu Q., Zhu L., Yin L., Hu C. and Chen L. Cell wall pectin and its binding capacity contribute to aluminium resistance in buckwheat [C]. The 2nd International Conference on Bioinformatics and Biomedical Engineering, 4508-4511. 2008.
 
[29]  Furukawa J., Yamaji N., Wang H., Mitani N., Murata Y., Sato K., Katsuhara M., Takeda K. and Ma J.F. An aluminum-activated citrate transporter in barley. Plant and Cell Physiology, 48:1081-1091, 2007.
 
[30]  Guenoune G.D., Elbaum M., Sagi G., Levy A. and Epel B.L. Tobacco mosaic virus (TMV) replicase and movement protein function synergistically in facilitating TMV spread by lateral diffusion in the plasmodesmal desmotubule of Nicotiana Benthamiana. Molecular Plant, 21:335-345, 2008.
 
[31]  Ahad A. and Nick P. Actin is bundled in activation-tagged tobacco mutants that tolerate aluminum. Planta, 225:451-468, 2007.
 
[32]  Ahn S.J., Sivaguru M., Chung G.C., Rengel Z. and Matsumoto H. Aluminium-induced growth inhibition is associated with impaired efflux and influx of H+ across the plasma membrane in root apices of squash (Cucurbita pepo). Journal of Experimental Botany, 53: 1959-1966, 2002.
 
[33]  Ahn S.J., Sivaguru M., Osawa H., Chung G.C. and Matsumoto H. Aluminum inhibits the H+-ATPase activity by permanently altering the plasma membrane surface potentials in squash roots. Plant Physiology, 126:1381-1390, 2001.
 
[34]  Ahn S.J., Rengel Z. and Mastsumoto H. Aluminum-induced plasma membrane surface potential and H+-ATPase activity in near-isogenic wheat lines differing in tolerance to aluminum. New Phytologist, 162:71-79, 2004.
 
[35]  Albrecht G. and Mustroph A. Sucrose utilization via invertase and sucrose synthase with respect to accumulation of cellulose and callose synthesis in wheat roots under oxygen deficiency. Russian Journal of Plant Physiology, 50:813-820, 2003.