Application of cell and tissue culture and in vitro selection for disease resistance breeding — a review

Euphytica ◽  
1991 ◽  
Vol 56 (3) ◽  
pp. 269-285 ◽  
Author(s):  
R. W. van den Bulk
2010 ◽  
Vol 9 (8) ◽  
pp. 437-446 ◽  
Author(s):  
Ramesh Chandra ◽  
Madhu Kamle ◽  
Anju Bajpai ◽  
M. Muthukumar ◽  
Shahina Kalim

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 572c-572
Author(s):  
James D. Kell

The use of RAPD markers in disease resistance breeding has been successfully demonstrated in horticultural crops. The identification of RAPD markers and their potential role in disease resistance breeding was first demonstrated in tomato; the procedure of bulk segregant analysis for detecting linkages between RAPD markers and genes conditioning resistance to downy mildew was described in lettuce; the use of linked RAPD markers to facilitate the efficient pyramiding of epistatic rust resistance genes to prolong their durability has been illustrated in common bean; the development of allele specific or sequence characterized primers linked to resistance genes has been achieved in pea, bean, tomato, and lettuce Indirect selection for disease resistance based on molecular markers is not a replacement for classical breeding procedures. Used as tools, markers offer breeders unique opportunities to combine resistance to an array of different pathogens and efficiently pyramid epistatic resistance genes for highly variable fungal pathogens. This would not always be possible in the absence of linked markers.


2018 ◽  
Vol 5 (2) ◽  
pp. 44-54 ◽  
Author(s):  
Veena S Anil ◽  
Savitha Lobo ◽  
Spurti Bennur

Somaclonal variations (SV) are genetic or epigenetic changes induced in plant cell and tissue culture. Induction of somaclonal variation, is an alternate approach to conventional breeding and transgenic approaches to introduce desirable genetic variability in the gene pool. SVs that occur spontaneously in culture induce changes in a range of plant characters. However, the probability of improving a key agronomic trait such as disease resistance can be cumbersome when left to chance alone. The efficiency of developing disease resistant SVs is better with the imposition of an appropriate in vitro selection pressure. Selection agents that have been applied include pathogen elicitors, pathogen culture filtrate and purified pathotoxins. This method of SV selection has been successful in enhancing disease resistance in several crops and it is an accepted biotechnological approach with tremendous potential for crop improvement.


2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Anthony J. Conner ◽  
Helen Searle ◽  
Jeanne M. E. Jacobs

Abstract Background A frequent problem associated with the tissue culture of Compositae species such as chicory (Cichorium intybus L.) and lettuce (Lactuca sativa L.) is the premature bolting to in vitro flowering of regenerated plants. Plants exhibiting such phase changes have poor survival and poor seed set upon transfer from tissue culture to greenhouse conditions. This can result in the loss of valuable plant lines following applications of cell and tissue culture for genetic manipulation. Results This study demonstrates that chicory and lettuce plants exhibiting stable in vitro flowering can be rejuvenated by a further cycle of adventitious shoot regeneration from cauline leaves. The resulting rejuvenated plants exhibit substantially improved performance following transfer to greenhouse conditions, with increased frequency of plant survival, a doubling of the frequency of plants that flowered, and substantially increased seed production. Conclusion As soon as in vitro flowering is observed in unique highly-valued chicory and lettuce lines, a further cycle of adventitious shoot regeneration from cauline leaves should be implemented to induce rejuvenation. This re-establishes a juvenile phase accompanied by in vitro rosette formation, resulting in substantially improved survival, flowering and seed set in a greenhouse, thereby ensuring the recovery of future generations from lines genetically manipulated in cell and tissue culture.


1987 ◽  
Vol 99 (2) ◽  
pp. 159-163 ◽  
Author(s):  
H. S. Chawla ◽  
G. Wenzel

1995 ◽  
pp. 19-26 ◽  
Author(s):  
F. Hammerschlag ◽  
D. Ritchie ◽  
D. Werner ◽  
G. Hashmil ◽  
L. Krusberg ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document