| dc.creator |
AlOlaby, Reem R. |
|
| dc.creator |
Zafarullah, Marwa |
|
| dc.creator |
Barboza, Mariana |
|
| dc.creator |
Peng, Gang |
|
| dc.creator |
Varian, Bernard J. |
|
| dc.creator |
Erdman, Susan E. |
|
| dc.creator |
Lebrilla, Carlito |
|
| dc.creator |
Tassone, Flora |
|
| dc.date |
2022-07-25T18:28:11Z |
|
| dc.date |
2022-07-25T18:28:11Z |
|
| dc.date |
2022-07-22 |
|
| dc.date |
2022-07-25T16:32:38Z |
|
| dc.date.accessioned |
2023-03-01T18:11:26Z |
|
| dc.date.available |
2023-03-01T18:11:26Z |
|
| dc.identifier |
https://hdl.handle.net/1721.1/144034 |
|
| dc.identifier |
Genes 13 (8): 1300 (2022) |
|
| dc.identifier |
PUBLISHER_CC |
|
| dc.identifier.uri |
http://localhost:8080/xmlui/handle/CUHPOERS/279091 |
|
| dc.description |
Environmental factors such as diet, gut microbiota, and infections have proven to have a significant role in epigenetic modifications. It is known that epigenetic modifications may cause behavioral and neuronal changes observed in neurodevelopmental disabilities, including fragile X syndrome (FXS) and autism (ASD). Probiotics are live microorganisms that provide health benefits when consumed, and in some cases are shown to decrease the chance of developing neurological disorders. Here, we examined the epigenetic outcomes in offspring mice after feeding of a probiotic organism, <i>Lactobacillus reuteri</i> (<i>L. reuteri</i>), to pregnant mother animals. In this study, we tested a cohort of Western diet-fed descendant mice exhibiting a high frequency of behavioral features and lower FMRP protein expression similar to what is observed in FXS in humans (described in a companion manuscript in this same GENES special topic issue). By investigating 17,735 CpG sites spanning the whole mouse genome, we characterized the epigenetic profile in two cohorts of mice descended from mothers treated and non-treated with <i>L. reuteri</i> to determine the effect of prenatal probiotic exposure on the prevention of FXS-like symptoms. We found several genes involved in different neurological pathways being differentially methylated (<i>p</i> ≤ 0.05) between the cohorts. Among the key functions, synaptogenesis, neurogenesis, synaptic modulation, synaptic transmission, reelin signaling pathway, promotion of specification and maturation of neurons, and long-term potentiation were observed. The results of this study are relevant as they could lead to a better understanding of the pathways involved in these disorders, to novel therapeutics approaches, and to the identification of potential biomarkers for early detection of these conditions. |
|
| dc.format |
application/pdf |
|
| dc.publisher |
Multidisciplinary Digital Publishing Institute |
|
| dc.relation |
http://dx.doi.org/10.3390/genes13081300 |
|
| dc.rights |
Creative Commons Attribution |
|
| dc.rights |
https://creativecommons.org/licenses/by/4.0/ |
|
| dc.source |
Multidisciplinary Digital Publishing Institute |
|
| dc.title |
Differential Methylation Profile in Fragile X Syndrome-Prone Offspring Mice after in Utero Exposure to Lactobacillus Reuteri |
|
| dc.type |
Article |
|
| dc.type |
http://purl.org/eprint/type/JournalArticle |
|