Callose Explained

Callose is a plant polysaccharide. Its production is due to the glucan synthase-like gene (GLS) in various places within a plant. It is produced to act as a temporary cell wall in response to stimuli such as stress or damage.[1] Callose is composed of glucose residues linked together through β-1,3-linkages, and is termed a β-glucan. It is thought to be manufactured at the cell wall by callose synthases and is degraded by β-1,3-glucanases. Callose is very important for the permeability of plasmodesmata (Pd) in plants; the plant's permeability is regulated by plasmodesmata callose (PDC). PDC is made by callose synthases and broken down by β-1,3-glucanases (BGs). The amount of callose that is built up at the plasmodesmatal neck, which is brought about by the interference of callose synthases (CalSs) and β-1,3-glucanases, determines the conductivity of the plasmodesmata.[2]

Formation and function

Callose is laid down at plasmodesmata, at the cell plate during cytokinesis, and during pollen development. Endothecium contains a substance callose, which makes it thicker. Callose is produced in response to wounding, infection by pathogens,[3] aluminium, and abscisic acid. When there is wounding in the plant tissue, it is fixed by the deposition of callose at the plasmodesmata and cell wall; this process happens within minutes after damage. Even though callose is not a constitutional component of the plant's cell wall, it is related to the plant's defense mechanism.[4] Deposits often appear on the sieve plates at the end of the growing season.[5] Callose also forms immediately around the developing meiocytes and tetrads of sexually reproducing angiosperms but is not found in related apomictic taxa.[6] Callose deposition at the cell wall has been suggested as an early marker for direct somatic embryogenesis from cortical and epidermal cells of Cichorium hybrids.[7] Temporary callose walls are also thought to be a barrier between a cell and its environment, while the cell is undergoing a genetic programming that allows it to differentiate.[8] This is because, callose walls can be found around nucellar embryos during Nucellar embryony.[9]

See also

Notes and References

  1. Book: 2016 . Callose . Hine R, Martin E . A Dictionary of Biology . Oxford University Press . 978-0-19-871437-8 . http://www.oxfordreference.com/view/10.1093/acref/9780198714378.001.0001/acref-9780198714378-e-6562 .
  2. De Storme N, Geelen D . Callose homeostasis at plasmodesmata: molecular regulators and developmental relevance . Frontiers in Plant Science . 5 . 138 . 2014 . 24795733 . 4001042 . 10.3389/fpls.2014.00138 . free .
  3. Nowicki . Marcin . Lichocka . Małgorzata . Nowakowska . Marzena . Kłosińska . Urszula . Kozik . Elżbieta U. . vanc . A Simple Dual Stain for Detailed Investigations of Plant-Fungal Pathogen Interactions . Vegetable Crops Research Bulletin . January 2012 . 77 . 1 . 61–74 . 10.2478/v10032-012-0016-z . free .
  4. Chen XY, Kim JY . Callose synthesis in higher plants . Plant Signaling & Behavior . 4 . 6 . 489–92 . June 2009 . 19816126 . 2688293 . 10.4161/psb.4.6.8359.
  5. Book: Hemsley. Alan R.. Bell. Peter R. . vanc . Green plants : their origin and diversity. 2000. Cambridge University Press. Cambridge. 978-0-521-64109-8. 2nd.
  6. Carman. John G.. Crane. Charles F.. Riera-Lizarazu. Oscar . vanc . Comparative Histology of Cell Walls during Meiotic and Apomeiotic Megasporogenesis in Two Hexaploid Australasian Elymus Species. Crop Science . 1991 . 31 . 6 . 1527 . 10.2135/cropsci1991.0011183X003100060029x .
  7. Dubois T, Guedira M, Dubois J, Vasseur J . Direct Somatic Embryogenesis in Roots of Cichorium: Is Callose an Early Marker?. Annals of Botany. May 1990. 65. 5. 539–545. 10.1093/oxfordjournals.aob.a087967.
  8. Tucker MR, Paech NA, Willemse MT, Koltunow AM . 2001 . Dynamics of callose deposition and β-1,3-glucanase expression during reproductive events in sexual and apomictic Hieracium. . Planta . 212 . 4 . 487–498 . 10.1007/s004250000445 . 11525505 . 12073031 .
  9. Gupta P, Shivanna KR, Mohan Ram HY . 1996 . Apomixis and polyembryony in the guggul plant, Commiphora wightii. . Ann Bot . 78 . 67–72 . 10.1006/anbo.1996.0097 .