Journal of Environmental BiologypISSN: 0254-8704 ; eISSN: 2394-0379 ; CODEN: JEBIDP |
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Abstract - Issue Nov 2010, 31 (6) BackUse of degenerate primers in
rapid generation of microsatellite markers in Panicum maximum 1National Research Centre on Plant Biotechnology, IARI, 2Crop Improvement Division, Indian Grassland and Fodder Research
Institute, (Received: Abstract: Guineagrass
(Panicum maximum Jacq.) is
an important forage grass of tropical and semi-tropical regions, largely apomictic and predominantly exist in tetraploid
form. For molecular breeding work, it is prerequisite to develop and design
molecular markers for characterization of genotypes, development of linkage map
and marker assisted selection. Hence, it is an important researchable issue to
develop molecular markers in those crops where such information is scanty.
Among many molecular markers, microsatellites or
simple sequence repeat (SSR) markers are preferred markers in plant breeding.
Degenerate primers bearing simple sequence repeat as anchor motifs can be
utilized in rapid development of SSR markers; however selection of suitable
degenerate primers is a prerequisite for such procedure so that SSR enriched
genomic library can be made rapidly.? In
the present study seven? degenerated? primers namely KKVRVRV(AG)10,
KKVRVRV(GGT)5, KKVRVRV(CT)10, KKVRVRV(AAT)6,
KKVRVRV(GTG)6, KKVRVRV(GACA)5 and KKVRVRV(CAA)6
were used in amplification of Panicum maximum? genomic DNA. Primers with repeat motifs? (GGT)5 and (AAT)6 have
not reacted whereas (AG)10, (GACA)5 and (CAA)6
highly informative as they have generated many DNA fragments ranging? from 250 to 1600 bps as revealed from the
results obtained with restriction digestion of recombinant plasmids. Primer
with (CT)10 anchor repeat, amplified fragments of high molecular
weight where as (GTG)6? primer
generated only? six bands with low
concentration indicating less suitability of these primer in SSR markers
development in P. maximum. Key
words: Degenerate primers, Microsatellite markers, Panicum
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