期刊
ACTA PHYSIOLOGIAE PLANTARUM
卷 36, 期 2, 页码 555-559出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s11738-013-1429-0
关键词
Genetic fidelity; Gene targeted; Molecular markers; Plant regeneration; Somaclonal variation
资金
- Council of scientific and industrial research (CSIR), New Delhi
- University grants commission (UGC), New Delhi
A newly developed and novel DNA marker technique, i.e. start codon targeted (SCoT) polymorphic markers that target plant gene regions were used to assess genetic stability of in vitro raised plants of Cleome gynandra multiplied by enhanced bud proliferation from nodal segments. Seven randomly selected micropropagated plants, following at least 2 months of growth in the greenhouse along with mother plant were subjected to molecular analysis. Of 24 primers screened, 15 primers produced unambiguous and reproducible bands. All 15 primers generated a total of 65 fragments, with a mean of 4.3 ranging 2-7 per primer. No polymorphism was detected in regenerated plants and the mother plant, revealing the genetic fidelity of the in vitro raised plantlets. To verify the results of SCoT analysis, random amplified polymorphic DNA (RAPD) markers were also used for the assessment of genetic fidelity of tissue culture raised plants. The monomorphic banding pattern in micropropagated plants and the mother plant obtained from SCoT and RAPD analysis confirms the genetic stability of the in vitro raised plants and demonstrates the reliability of our micropropagation system for C. gynandra, an important C-4 plant.
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