Transient Gene Expression in Catharanthus roseus Flower Petals Using Agroinfiltration.

Agroinfiltration Catharanthus roseus Gene expression analysis Regulation of specialized metabolism Transient transformation

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2022
Historique:
entrez: 22 6 2022
pubmed: 23 6 2022
medline: 25 6 2022
Statut: ppublish

Résumé

Transient transformation methods are frequently used to determine gene function. However, until recently only a few methods have been available in the model medicinal plant Catharanthus roseus. Here, we describe a rapid and highly reproducible protocol for the overexpression of genes of interest by agroinfiltration of C. roseus flower petals. This high throughput method is particularly suitable for screening purposes, for instance, target gene screening of transcription factor candidates, and complements other available methods.

Identifiants

pubmed: 35732952
doi: 10.1007/978-1-0716-2349-7_20
doi:

Substances chimiques

Plant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

281-291

Informations de copyright

© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Références

van der Fits L, Memelink J (1997) Comparison of the activities of CaMV 35S and FMV 34S promoter derivatives in Catharanthus roseus cells transiently and stably transformed by particle bombardment. Plant Mol Biol 33:943–946
doi: 10.1023/A:1005763605355
Bhadra R, Vani S, Shanks JV (1993) Production of indole alkaloids by selected hairy root lines of Catharanthus roseus. Biotechnol Bioeng 41:581–592
doi: 10.1002/bit.260410511
Weaver J, Goklany S, Rizvi N et al (2014) Optimizing the transient FAST agro-mediated seedling transformation (FAST) method in Catharanthus roseus seedlings. Plant Cell Rep 33:89–97
doi: 10.1007/s00299-013-1514-2
Verweij W, Spelt C, Di Sansebastiano G-P et al (2008) An H+ P-ATPase on the tonoplast determines vacuolar pH and flower colour. Nat Cell Biol 10:1456–1462
doi: 10.1038/ncb1805
Yasmin A, Debener T (2010) Transient gene expression in rose petals via Agrobacterium infiltration. Plant Cell Tissue Organ Cult 102:245–250
doi: 10.1007/s11240-010-9728-2
Shang Y, Schwinn KE, Bennett MJ et al (2007) Methods for transient assay of gene function in floral tissues. Plant Methods 3:1
doi: 10.1186/1746-4811-3-1
Van Moerkercke A, Steensma P, Gariboldi I et al (2016) The basic helix-loop-helix transcription factor BIS2 is essential for monoterpenoid indole alkaloid production in the medicinal plant Catharanthus roseus. Plant J 88:3–12
doi: 10.1111/tpj.13230
Pan Q, Wang C, Xiong Z et al (2019) CrERF5, an AP2/ERF transcription factor, positively regulates the biosynthesis of Bisindole alkaloids and their precursors in Catharanthus roseus. Front Plant Sci 10:931
doi: 10.3389/fpls.2019.00931
Singh SK, Patra B, Paul P et al (2020) Revisiting the ORCA gene cluster that regulates terpenoid indole alkaloid biosynthesis in Catharanthus roseus. Plant Sci 293:110408
doi: 10.1016/j.plantsci.2020.110408
Courdavault V, Papon N, Clastre M et al (2014) A look inside an alkaloid multisite plant: the Catharanthus logistics. Curr Opin Plant Biol 19:43–50
doi: 10.1016/j.pbi.2014.03.010
van Der Heijden R, Jacobs DI, Snoeijer W et al (2004) The Catharanthus alkaloids: pharmacognosy and biotechnology. Curr Med Chem 11:607–628
doi: 10.2174/0929867043455846
Schweizer F, Colinas M, Pollier J et al (2018) An engineered combinatorial module of transcription factors boosts production of monoterpenoid indole alkaloids in Catharanthus roseus. Metab Eng 48:150–162
doi: 10.1016/j.ymben.2018.05.016
Karimi M, Inze D, Depicker A (2002) GATEWAY vectors for agrobacterium-mediated plant transformation. Trends Plant Sci 7:193–195
doi: 10.1016/S1360-1385(02)02251-3
Sarrion-Perdigones A, Vazquez-Vilar M, Palací J et al (2013) GoldenBraid 2.0: a comprehensive DNA assembly framework for plant synthetic biology. Plant Physiol 162:1618–1631
doi: 10.1104/pp.113.217661
Pollier J, Vanden Bossche R, Rischer H, Goossens A (2014) Selection and validation of reference genes for transcript normalization in gene expression studies in Catharanthus roseus. Plant Physiol Biochem 83:20–25
doi: 10.1016/j.plaphy.2014.07.004
Munkert J, Pollier J, Miettinen K et al (2015) Iridoid synthase activity is common among the plant progesterone 5beta-reductase family. Mol Plant 8:136–152
doi: 10.1016/j.molp.2014.11.005

Auteurs

Maite Colinas (M)

Department of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology, Jena, Germany. mmartinez@ice.mpg.de.

Alain Goossens (A)

Ghent University, Department of Plant Biotechnology and Bioinformatics, Ghent, Belgium. Alain.Goossens@psb.vib-ugent.be.
VIB Center for Plant Systems Biology, Ghent, Belgium. Alain.Goossens@psb.vib-ugent.be.

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