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Parikh, I.

Publications and source records attributed to Parikh, I..

2 recordsLinked to original sources

Non-uniform chromosomal SNP density biases sites of meiotic crossovers in Drosophila melanogaster

Here we localize a genetic suppressor that enhances the reduced locomotor activity phenotype of flies lacking brain dopamine. We utilized a non-bulked segregant analysis using whole genome sequencing (WGS), mapping the trait to a roughly 3.5 mega-base (Mb) region of the X-chromosome. However, this mapping yielded [~]5-fold lower resolution than anticipated, due to an uneven distribution of Single Nucleotide Polymorphisms (SNPs) between the X-chromosomes of the two recombining lines. This uneven SNP distribution was associated with recombination events biased towards regions of low SNP density, and away from the more SNP dense regions associating with the activity phenotype. We find that nearly perfect mapping of X-chromosome visible markers occurs only in historical data from a time before the establishment of discrete genetic background strains. This suggests that genetic uniformity in early Drosophila studies may have contributed to more consistent recombination frequencies, whereas modern mapping efforts are complicated by variability in SNP distribution across recombining strains. These findings highlight challenges in Drosophila genetic mapping in situations where altered SNP density can skew recombination, complicating trait localization. Article SummaryGenetic mapping studies generally assume uniform crossover distribution across chromosomes. However, this study demonstrates that an uneven density of single nucleotide polymorphism (SNP) is associated with biased sites of meiotic recombination. Using brain dopamine-deficient Drosophila, SNP dense regions show reduced crossover frequency, which reduced the mapping resolution, complicating genetic trait localization. These findings highlight the need to consider parental chromosome SNP distribution and its impact on recombination when designing genetic mapping studies. Future studies should consider chromosome structure, parental haplotype, and sequence heterogeneity to enhance mapping accuracy and resolution.

genetics↗

Female mice are resilient to age-related decline of substantia nigra dopamine neuron firing parameters

The degeneration of substantia nigra (SN) dopamine neurons is a central feature in the pathology associated with Parkinsons disease, which is characterized by progressive loss of motor and cognitive functions. The largest risk factors for Parkinsons disease are age and sex; most cases occur after age 60 and males have nearly twice the incidence as females. While much research in Parkinsons has focused on the mechanisms underlying dopamine neuron degeneration, very little work has considered the influence of these two risk factors to disease risk and presentation. In this work, we performed whole cell patch clamp recordings in brain slices to study the alterations in intrinsic firing properties of single dopamine neurons in C57BL/6 mice across ages and between sexes. We observed a progressive decline in dopamine neuron firing activity in males by 18 months of age, while dopamine neurons from females remained largely unaffected. A semiquantitative analysis of midbrain dopamine neuron populations revealed a slight decrease only in substantia nigra dopamine neurons in males, while females did not change. This was also accompanied by increases in the expression of genes that have been linked to Parkinsons including PTEN-induced kinase 1 (PINK1) in both males and females, and the ubiquitin ligase parkin, primarily in the substantia nigra of males. These impairments in dopamine neuron function in males may represent a vulnerability to further insults that could predispose these cells to neurodegenerative diseases such as in Parkinsons.

neuroscience↗