Search bioRxiv⌕ Search

Biology subjects

Fraccaroli, I.

Publications and source records attributed to Fraccaroli, I..

3 recordsLinked to original sources

Opposing behavioral roles for a single gene in a species with a supergene polymorphism

Behavioral trade-offs, such as between territorial aggression and parental care, require coordination among neural and genetic mechanisms that influence opposing phenotypes. In some systems, including the white-throated sparrow, this coordination has been proposed to be mediated in part by chromosomal inversions that bind together multiple genes associated with alternative strategies. Here, we demonstrate that opposing components of a life-history trade-off can be linked, via alternative alleles inside a chromosomal rearrangement, to a single pleiotropic gene. In white-throated sparrows, a species with polymorphic aggressive and parental behavior, the gene encoding the neuromodulator vasoactive intestinal peptide (VIP) lies within an inversion-based supergene. Working with a free-living population, we found that VIP expression in a pro-aggression cell population in the anterior hypothalamus positively predicted territorial singing, whereas expression in a pro-parental cell population in the infundibular nucleus positively predicted parental provisioning. Expression in these two regions was negatively correlated, consistent with opposing behavioral roles. Allele-specific analyses revealed stronger expression bias toward the supergene-associated allele in the anterior hypothalamus than in the infundibular nucleus. These findings suggest that chromosomal inversions can support opposing behavioral phenotypes not only by linking multiple genes, but also by driving regulatory divergence of individual genes that organize behavioral trade-offs.

neuroscience↗

APP-KI mice do not display the hallmark age-dependent cognitive decline of amyloid diseases

APP knock-in (KI) mice serve as an exciting new model system to understand amyloid beta (A{beta}) pathology, overcoming many of the limitations of previous overexpression-based model systems. The APPSAA mouse model (containing the humanized APP with three familial Alzheimers disease mutations) and the APPWT control are the first commercially available APP KI mice within the United States. While APPSAA mice have been shown to develop progressive A{beta} pathology and neuroinflammation, behavioral changes, particularly in cognitive functions, have yet to be described. Therefore, we performed an in-depth longitudinal study over 12 months, assessing cognition in these two strains, as well as assessments of motor and GI function. We surprisingly note no overt, progressive cognitive impairment or motor deficits. However, we do observe a significant increase in fecal output in APPSAA mice compared to APPWT at 12 months old. These data provide a baseline for these models behavioral attributes. HighlightsO_LIAPPSAA and APPWT knock-in mice do not display age related cognitive decline C_LIO_LIFecal output appears altered by APP genotype, but no other measure of GI function is impacted. C_LIO_LIBoth genotypes behave equally in motor function tests C_LI

neuroscience↗

Overexpression of human alpha-synuclein leads to dysregulated microbiome and metabolites with ageing in a rat model of Parkinson disease

Since Braaks hypothesis stating that sporadic Parkinsons disease follows a specific progression of the pathology from the peripheral to the central nervous system and can be monitored by detecting accumulation of the alpha-Synuclein protein. There is growing interest in understanding how the gut (commensal) microbiome can regulate alpha-Synuclein accumulation which can lead to PD. We studied a transgenic rat model overexpressing the human alpha-Synuclein and found that the protein overexpression resulted in gut alpha-Synuclein expression and aggregation in the gut neurons with advancing age. A progressive gut microbial composition alteration characterized by the reduction of Firmicutes to Bacteroidetes ratio could be detected in the young transgenic rat model and interestingly this ratio was then increased with aging. This observation was accompanied in older animals by intestinal inflammation, increase gut permeability and a robust alteration in metabolites production characterized by the increase of succinate level in the feces and serum. Manipulation of the gut bacteria by short-term antibiotics treatment revealed a complete loss of short-chain fatty acids (SCFAs) and reduction in succinate levels. Although antibiotics treatment did not change alpha-synuclein expression in the enteric nervous system of the colon, it can reduce alpha-synuclein expression in the olfactory bulb of the transgenic rats. In summary, synchronous with ageing, our data emphasize that the gut microbiome dysbiosis leads to a specific alteration of gut metabolites which are reflected in the serum and can be modulated by the environment.

neuroscience↗