Literature DB >> 14543736

Physical methods for the transformation of plant cells.

J H Oard1.   

Abstract

Transfer and expression of foreign genes in adult plants and their progeny has been achieved by acceleration of DNA-coated particles or microinjection techniques. Cultured cells or embryoids served as targets for the introduction of marker genes that were stably expressed in the nucleus or the chloroplast. Cloned genes from the maize anthocyanin pathway were regulated in a tissue-specific manner when transferred into maize by particle acceleration. In spite of these successes, stable transformation efficiency was low due to uneven particle distribution and cell death after bombardment. Transferred genes did not always segregate in a Mendelian fashion in the succeeding generation, and additional efforts of embryo rescue or shoot grafts were needed to obtain viable progeny from original transformants. New technical advances such as the helium-driven particle gun may improve transformation rates in the future, but some problems of cell manipulation remain.

Entities:  

Year:  1991        PMID: 14543736     DOI: 10.1016/0734-9750(91)90401-g

Source DB:  PubMed          Journal:  Biotechnol Adv        ISSN: 0734-9750            Impact factor:   14.227


  3 in total

1.  Transient expression of gus gene in intact seed embryos of Indica rice after electroporation-mediated gene delivery.

Authors:  A Chaudhury; S C Maheshwari; A K Tyagi
Journal:  Plant Cell Rep       Date:  1995-01       Impact factor: 4.570

Review 2.  Perspectives on new opportunities for nano-enabled strategies for gene delivery to plants using nanoporous materials.

Authors:  Mohsen Niazian; Ayoub Molaahmad Nalousi; Pejman Azadi; Leila Ma'mani; Stephen F Chandler
Journal:  Planta       Date:  2021-09-24       Impact factor: 4.116

3.  A rapid method to monitor DNA precipitation onto microcarriers before particle bombardment.

Authors:  I J Ratnayaka; J H Oard
Journal:  Plant Cell Rep       Date:  1995-10       Impact factor: 4.570

  3 in total

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