Abstract:
The present study was conducted on different accessions of Moraceae to
evaluate the genetic variation in them on the basis of morphological and biochemical
attributes as well as by using molecular markers (SSR and ISSR). The developmental
genes cup shaped cotyledons (CUC2) were also studied in order to confirm their
functional status. For morphological, biochemical and molecular studies mulberry fresh
leaves were taken and all the parameters were taken in replicates. Morphologically
leaves of the majority of the accessions had light green color, acute tip, and soft surface
along with cordate shaped leaves. The others had lobed shape, dark color, doubly
serrate or dentate, acuminate and coarse leaves. There were significant differences in
means of lamina length, lamina width and leaf area index. In biochemical analysis, the
carbohydrates content was the highest in Korean subni (3.7626±0.204 cm) followed by
Morus nigra(3.728±0.1795 cm), Morus latefolia (3.643±0.2458 cm) and P.F.I
(3.568±0.3057 cm). Punjab II (1.704±0.1695 cm) showed the lowest carbohydrates
content. The protein contents of Kanmasi Japan (1.7007±0.0049 cm) were higher as
compared to Punjab-II-punjab (1.4030±0.0455 cm). The higher values of carbohydrate
and protein content revealed that the leaves had the more palatability for silkworms.
Lun-40-punjab showed the highest total phenolic content. Phenolic play a key role in
traditional medicines. The maximum IC50 value was of Morus indica(172.21 mg/g)
followed by Morus alba(152.7 mg/g) and PFI (122.4 mg/g). Punjab II Punjab (11.6),
Kanmasi Japan (11.5) showed the minimum and same amount of anti-oxidant activity.
One of the developmental genes CUC2 was observed in seven Morus strains.
This strategy produced good-quality sequences, which were analyzed and compared to
each other and to theCUC2c sequence of the reference M. notabilis strain.The
sequencing results showed that the mean distance present in the overall sequence pairs
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was 0.017. Molecular diversity between thirty accessions was checked through DNA
markers i.e. SSR and ISSRs by the use of different softwares (NTSYS PC 2.2, Minitab,
Statista, R) The SSRs produced 15 polymorphic bands out of 25 (60%) SS18 and
MULSTR1 showed best results with the highest PIC and hundred percent
polymorphism while the least was shown by SS04. It was also obvious that pic of SSR
was somehow less than ISSR. The analysis of molecular variance (AMOVA) gave P
value of 0.6434. The ISSR markers showed more polymorphism with more PIC value.
The P value obtained from the results was 0.1089, while CV was 35.7. Our diversity
results proved that all group were somewhat distant