Explain the conventional way to prove the true-to-type nature of a clonal plant.
Several researches
which examine clonal fidelity use the same two approaches: ISSR (inter simple sequence repeat) and RAPD (Random Amplification of Polymorphic DNA) (Alizadeh & Singh, 2009; Rawat, Rawat, Mehrotra, Chandra, &
Nautiyal, 2013; Yadav, Aggarwal, & Singh, 2013). Therefore I consider these two methods as the common way to examine
this issue.
For which reasons is mass propagation of Gloriosa such a promising technique and genetic fidelity so important?
Gloriosa is an
old medicine plant which has been used for a long time in both Africa and Asia.
The plant contains an alkaloid called colchicine. This substance is able to
inhibit mitosis and is used to treat acute gout (Bajaj, 2012).
Gloriosa is more and more used to produce colchicine through mass propagation (Yadav et al., 2013).
Since it is used for medication it is important that the substances of
content of the plant stay the same.
Explain the terms somaclonal variants, PCR, Primer, amplification, genetic markers.
Somaclonal variants
Somaclonal
variants are new genetic different cells which appear randomly when cells
reproduce themselves. This happens particularly when the cells are in vitro
clonal propagated.(Jaligot et al., 2011)
PCR
Polymerase Chain
Reaction (PCR) is a method to copy pieces of DNA. That for the DNA is heated to
separate the twin strings. Then it is blended with synthetic primers which
attach to certain areas of the single strings. Then enzymes extend the starters until there is
another double string. (Duran,
2000)
Primer
A Primer is a
short piece of single stringed DNA which attaches to a certain area of a single string of DNA. It
is the starting point for the DNA polymerase to build the second string.(‘Primer, Starter |
Biologie-Definitionen online’, 2013)
Amplification
Amplification
means the multiplication of DNA fragments by artificial copying (‘DNA amplification’, 2003).
Genetic Marker
A sequence of
DNA which is located on a known place of the chromosome (National Institutes of Health, n.d.).
Is the proposed method save enough to prove genetic fidelity of clonal propagated plants?
Yadav et al. (2013)
confirm, that these ISSR and RAPD are convenient to prove genetic stability of mass
propagated Gloriosa. As in so many studies (see question 1) these are
the preferred methods to prove genetic fidelity, I assume that they are save
enough.
Literature:
Alizadeh, M., & Singh, S. K. (2009).
Molecular assessment of clonal fidelity in micropropagated grape (Vitis spp.)
rootstock genotypes using RAPD and ISSR markers. Iranian Journal of
Biotechnology, 7(1), 37–44.
Bajaj, Y.
P. S. (2012). Medicinal and Aromatic Plants II. Springer Berlin
Heidelberg. Retrieved from https://books.google.ch/books?id=kofuCAAAQBAJ
DNA
amplification. (2003). Miller-Keane Encyclopedia and Dictionary of Medicine,
Nursing, and Allied Health. Retrieved from http://medical-dictionary.thefreedictionary.com/DNA+amplification
Duran, E.
A. (2000, April 1). Wissenschaft im Alltag: Die
Polymerase-Kettenreaktion. Retrieved
11 March 2017, from
http://www.spektrum.de/magazin/wissenschaft-im-alltag-die-polymerase-kettenreaktion/826243
Jaligot,
E., Adler, S., Debladis, É., Beulé, T., Richaud, F., Ilbert, P., … Rival, A.
(2011). Epigenetic imbalance and the floral developmental abnormality of the in
vitro-regenerated oil palm Elaeis guineensis. Annals of Botany, 108(8),
1453–1462. https://doi.org/10.1093/aob/mcq266
National
Institutes of Health. (n.d.). Talking Glossary of Genetic Terms. Retrieved from
https://www.genome.gov/glossary/index.cfm?id=86
Primer, Starter | Biologie-Definitionen
online. (2013, March 17).
Retrieved 11 March 2017, from http://www.biologie-lexikon.de/lexikon/primer.php
Rawat, J.
M., Rawat, B., Mehrotra, S., Chandra, A., & Nautiyal, S. (2013). ISSR and
RAPD based evaluation of genetic fidelity and active ingredient analysis of
regenerated plants of Picrorhiza kurroa. Acta Physiologiae Plantarum, 35(6),
1797–1805. https://doi.org/10.1007/s11738-013-1217-x
Yadav, K.,
Aggarwal, A., & Singh, N. (2013). Evaluation of genetic fidelity among
micropropagated plants of Gloriosa superba L. using DNA-based markers — a potential
medicinal plant. Fitoterapia, 89, 265–270.
https://doi.org/10.1016/j.fitote.2013.06.009
Hello Alessandro
AntwortenLöschenIt was interesting to read your blog. You found many different sources to answer the relevant questions in a short and precise way. In addition, your definitions of the important terms provide the needed information to understand the whole issue of mass propagation and gene fidelity better.
Regards, Bettina
Dear Alessandro
AntwortenLöschenThe blog was very enjoyable to read since the language is straight forward and the text to the point.
From an e-Mail of Hans-Ruedi Keller I understood that your answer to question Nr.1 is right, looking at it from a genomic level. He also explained that in traditional propagation programs time consuming in vivo cultures to test genomic stability is standard. However the literature list shows that you researched well.
From your text it becomes clear why genetic fidelity is important, but I missed the aspect that mass propagation is very promising because the other ways are much slower.
Altogether I enjoyed reading your blog and especially the definitions are explained very clearly.
Regards, Mirjam
Hi
AntwortenLöschenI found the explanations of the different terms short and well comprehensible.
The wide range of literature used shows a thorough reserch.
For question 2 you could have mentioned, that in vitro propagation protects the wild plants from being exploited.
kind regards,
Sandra
Hi Alessandro, it might be the last blog I comment and mark tonight - and it is probably the shortest and most concise I met today. Well done and well referenced. As Mirjam notes beside these molecular techniques true to type proof is traditionally done by in vivo cultures (and still is in most cases). And this is time consuming process and for colchicine tracking quite complex. Did you know of how toxic colchicine is? Cheers Hansruedi
AntwortenLöschen