Chemotropism
Chemotropism is defined as the growth of organisms navigated by chemical stimulus from outside of the organism. It has been observed in bacteria, plants and fungi.[1] A chemical gradient can influence the growth of the organism in a positive or negative way. Positive growth is characterized by growing towards a stimulus and negative growth is growing away from the stimulus.[2]
Chemotropism is slightly different from Chemotaxis, the major difference being that chemotropism is related to growth, while chemotaxis is related to locomotion. A chemotropic process may have an underlying chemotactic component, as is the case with mating yeast.[3]
Chemotropism in plants
One prime example of chemotropism is seen in plant fertilization and pollen tube elongation of angiosperms, flowering plants.[4] Unlike animals, plants cannot move, and therefore need a delivery mechanism for sexual reproduction. Pollen, which contains the male gametophyte is transferred to another plant via insects or wind.[5] If the pollen is compatible it will germinate and begin to grow.[5] The ovary releases chemicals that stimulates a positive chemotropic response from the developing pollen tube.[6] In response the tube develops a defined tip growth area that promotes directional growth and elongation of the pollen tube due to a calcium gradient.[5] The steep calcium gradient is localized in the tip and promotes elongation and orientation of the growth.[5] This calcium gradient is essential for the growth to occur; it has been shown that inhibiting the formation of the gradient results in no growth.[5] As the pollen tube continues to grow towards the ovules, the male sperm remains in the apical region and is transported to the female ovule.[7] The pollen tube elongates at a rate comparable to neurite development
An example of positive and negative chemotropism is shown by a plant's roots; the roots grow towards useful minerals displaying positive chemotropism, and grow away from harmful acids displaying negative chemotropism.[8][9]
Chemotropism in animals
In more complex organisms an example of chemotropic movement includes the growth of individual neuronal cell axons in response to extracellular signals.[10] Secreted protein can either repel or attract specific neurons. Some signal proteins such as netrins, semaphorins, neurotrophins and fibroblast growth factors have been identified in aiding neuronal growth.[10] These signals guide the developing axon to innervate the correct target tissue.[11] The neuronal growth cones are guided by gradients of chemoattractant molecules released from their intermediate or final targets. There is evidence that the axons of peripheral neurons are guided by chemotropism and the directed growth of some central axons is also a chemotropic response, it remains to be determined whether chemotropism also operates in the central nervous system. Evidence has also been noted in neuronal regeneration, where chemotropic substances guide the ganglionic neurites towards the degenerated neuronal stump.[12]
Chemotropism in Fungi
Fungal chemotropism was first reported over 100 years ago by Anton de Bary.[13] One example of fungi using chemotropism is seen in Yeast.Yeast release chemical pheromones in order to attract mates.[14] Each haploid yeast cells express specific haploid genes; haploid α-cells express α-genes and haploid a-cells express a-genes.[15] Each cell type releases a unique pheromone: a- or α-factor.[16] By secreting these factors a chemical gradient is formed that attracts the other type of yeast cell during mating. In order for the yeast to sense the gradient they have to have proper receptors that bind a- or α-factor: Ste3 and Ste2 respectively.[17] The receptors to detect the pheromones are seven transmembrane G-protein coupled receptor (GPCR).[16] Once activated, there is a signaling cascade that results in the activation of transcription factors for mating-specific genes such as those involved in cell cycle arrest, directional polarization towards the chemical gradient, and sexual hyphae formation.[13][17] When fungal hyphae touch, the cells merge to form a diploid zygote.[17] Mating pairs of budding yeast cells may polarize away from each other, but are able to adjust the location of polarity to enable successful alignment and fusion.[3]
See also
References
- ^ Turrà, David; El Ghalid, Mennat; Rossi, Federico; Di Pietro, Antonio (2015). "Fungal pathogen uses sex pheromone receptor for chemotropic sensing of host plant signals". Nature. 527 (7579): 521–524. Bibcode:2015Natur.527..521T. doi:10.1038/nature15516. ISSN 0028-0836. PMID 26503056. S2CID 4449720.
- ^ "Chemotropism Definition and Examples - Biology Online Dictionary". Biology Articles, Tutorials & Dictionary Online. 2019-10-07. Retrieved 2020-03-23.
- ^ a b Ghose, Debraj; Jacobs, Katherine; Ramirez, Samuel; Elston, Timothy; Lew, Daniel (2021-06-01). "Chemotactic movement of a polarity site enables yeast cells to find their mates". Proceedings of the National Academy of Sciences. 118 (22): e2025445118. Bibcode:2021PNAS..11825445G. doi:10.1073/pnas.2025445118. ISSN 0027-8424. PMC 8179161. PMID 34050026. S2CID 235242389.
- ^ "Pollen Tube: Growth, Function & Formation - Video & Lesson Transcript". Study.com. Retrieved 2020-04-18.
- ^ a b c d e Krichevsky, Alexander; Kozlovsky, Stanislav V.; Tian, Guo-Wei; Chen, Min-Huei; Zaltsman, Adi; Citovsky, Vitaly (2007-03-15). "How pollen tubes grow". Developmental Biology. 303 (2): 405–420. doi:10.1016/j.ydbio.2006.12.003. ISSN 0012-1606. PMID 17214979.
- ^ Reger, BJ; Chaubal, R; Pressey, R (1992). "Chemo-tropic responses by pearl millet pollen tubes". Sexual Plant Reproduction. 5 (1): 47–56. doi:10.1007/BF00714557. S2CID 4592052. Retrieved 7 February 2018.
- ^ Hepler, Peter K.; Vidali, Luis; Cheung, Alice Y. (2001-11-01). "Polarized Cell Growth in Higher Plants". Annual Review of Cell and Developmental Biology. 17 (1): 159–187. doi:10.1146/annurev.cellbio.17.1.159. ISSN 1081-0706. PMID 11687487.
- ^ Henke, Michael; Sarlikioti, Vaia (3 August 2014). "Exploring root developmental plasticity to nitrogen with a three-dimensional architectural model". Plant Soil. 385 (1–2): 49–62. doi:10.1007/s11104-014-2221-7. S2CID 17630453.
- ^ Newcombe FC, Rhodes AL (1904). "Chemotropism of Roots". Botanical Gazette. 37 (1): 22–35. doi:10.1086/328441. JSTOR 2465652. S2CID 84789317.
- ^ a b Song, Hong-jun; Poo, Mu-ming (March 2001). "The cell biology of neuronal navigation". Nature Cell Biology. 3 (3): E81–E88. doi:10.1038/35060164. ISSN 1476-4679. PMID 11231595. S2CID 7449327.
- ^ Tessier-Lavigne, Placzek, Lumsden, Dodd, Jessell (1988). "Chemotropic guidance of developing axons in the mammalian central nervous system". Nature. 336 (6201): 775–8. Bibcode:1988Natur.336..775T. doi:10.1038/336775a0. PMID 3205306. S2CID 4247407.
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: CS1 maint: multiple names: authors list (link) - ^ Gu X, Thomas PK, King RH (1995). "Chemotropism in nerve regeneration studied in tissue culture". Journal of Anatomy. 186 (1): 153–63. PMC 1167281. PMID 7649810.
- ^ a b Turrà, David; Nordzieke, Daniela; Vitale, Stefania; El Ghalid, Mennat; Di Pietro, Antonio (2016-09-01). "Hyphal chemotropism in fungal pathogenicity". Seminars in Cell & Developmental Biology. Transcriptional Enhancers. 57: 69–75. doi:10.1016/j.semcdb.2016.04.020. ISSN 1084-9521. PMID 27150623.
- ^ Martin, Sophie G. (2019-06-01). "Molecular mechanisms of chemotropism and cell fusion in unicellular fungi". Journal of Cell Science. 132 (11): jcs230706. doi:10.1242/jcs.230706. ISSN 0021-9533. PMID 31152053.
- ^ Lodish, Harvey; Berk, Arnoldaa; Zipursky, S. Lawrence; Matsudaira, Paul; Baltimore, David; Darnell, James (2000). "Cell-Type Specification and Mating-Type Conversion in Yeast". Molecular Cell Biology. 4th Edition.
- ^ a b Arkowitz, Robert A. (August 2009). "Chemical Gradients and Chemotropism in Yeast". Cold Spring Harbor Perspectives in Biology. 1 (2): a001958. doi:10.1101/cshperspect.a001958. ISSN 1943-0264. PMC 2742094. PMID 20066086.
- ^ a b c Merlini, Laura; Dudin, Omaya; Martin, Sophie G. (March 2013). "Mate and fuse: how yeast cells do it". Open Biology. 3 (3): 130008. doi:10.1098/rsob.130008. ISSN 2046-2441. PMC 3718343. PMID 23466674.