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Biology subjects

J, B.

Publications and source records attributed to J, B..

2 recordsLinked to original sources

Genetic diversity and evidence of recombination of Horsegram yellow mosaic virus infecting pole bean (Phaseolus vulgaris L.) from South India

The yellow mosaic disease (YMD) caused by begomoviruses is a major constraint for the production of pole bean (Phaseolus vulgaris L.) in India. Survey was carried out in the eastern dry zone of Karnataka during 2019-20 to record the incidence of yellow mosaic disease in pole bean which revealed the ubiquitous prevalence of YMD in pole bean ranging from 6.02 to 80.74 per cent. Leaf samples collected (symptomatic and asymptomatic) were subjected for begomovirus detection using specific primers. Twelve samples, representing all the 12 taluks in the surveyed region were considered for full genome amplification by RCA, cloned and sequenced. Genome length of 12 current isolates ranged from 2718 - 2744 and 2668 - 2671 nucleotides for DNA-A and DNA-B, respectively. Sequence analysis using Sequence Demarcation Tool (SDT) showed >91 per cent nucleotide identity of current isolates (DNA-A) with other horsegram yellow mosaic virus (HgYMV) isolates available in the GenBank. As per existing ICTV criteria, all the current isolates can be considered as strains of HgYMV. Further, DNA-B associated with all the 12 isolates also shared >91 per cent nucleotide identity with DNA-B of HgYMV isolates, indicating absence of component re-assortment in HgYMV. Variation in the pairwise nucleotide identity and phylogenetic analysis confirmed the existence of new strains within the current HgYMV isolates. GC plot analysis reveals potential recombination in the low GC rich regions. Further, recombination breakpoint analysis indicated intra-species recombination in both DNA-A and DNA-B, which might have driven the origin of new strains in HgYMV. This is the first comprehensive study on begomoviruses ioslates associated with the yellow mosaic disease of pole bean based on complete genome sequencing in the world.

molecular biology↗

Clustered Loss of Dendritic Spines Characterizes Encoding of Related Memory

Generation of new spines is often thought of as a correlate of memory and loss of spines is considered representing memory loss. Contrary to common belief, we observe that spine loss has functional value in distinctly encoding related life events rather than causing memory loss. Using spatial autocorrelation of dendritic morphology obtained from in vivo longitudinal imaging, we show that clustered loss, rather than gain, of new spines characterizes the formation of related memory. This spatially selective dendritic spine loss occurs closer to new spines formed during the acquisition of initial memory. Thus, enabling the dendrites to store multiple memories and their inter relationship. Remarkably, we find acquisition of related memory in the absence of NMDAR activation increases the fraction of such correlated spine loss.

neuroscience↗