000			02129nam a2200277Ia 4500
003			MX-MdCICY
005			20250625162441.0
040			_cCICY
090			_aB-20003
245	1	0	_aProtoplast isolation and transient gene expression in different petunia cultivars
490	0		_vProtoplasma, 260(1), p.271-280, 2023
520	3		_aThe protocol optimized for Petunia hybrida cv. Mirage Rose produced high protoplast yields in 3 out of other 11 cultivars (Damask White, Dreams White, and Opera Supreme White). Factors optimized in the protoplast transfection process showed that the best transfection efficiency (80 percent)was obtained using 2.5?×?105 protoplast density, 40 percent polyethylene glycol (PEG)concentration, 10 µg plasmid DNA, and 15 min of transfection time. Assessing the usability of the protocol for other cultivars (Damask White, Dreams White, and Opera Supreme White), a reasonable protoplast transfection efficiency (?50 percent)was observed in the cultivars Dreams White and Opera Supreme White, with lower efficiency (?50 percent)observed in the cv. Damask White. The transient expression of enhanced green fluorescent protein (eGFP)in the nucleus of the transfected protoplasts of all cultivars was confirmed using PCR. This system could be valuable for genome editing of unwanted genes in petunias using the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (Cas9)technology. Furthermore, it could contribute to other studies on protein subcellular localization, protein-protein interactions, and functional gene expression in the petunias.
650	1	4	_aEGFP
650	1	4	_aPCR
650	1	4	_aPETUNIA CULTIVARS
650	1	4	_aPROTOPLAST ISOLATION
650	1	4	_aTRANSFECTION EFFICIENCY
700	1	2	_aKang, H.
700	1	2	_aNaing, A. H.
700	1	2	_aPark, S. K.
700	1	2	_aChung, M. Y.
700	1	2	_aKim, C. K.
856	4	0	_uhttps://drive.google.com/file/d/1nSVwM9LaLQmmyulb-ZqieX4oRDby5_8p/view?usp=drivesdk _zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
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