The literature implies that Multiple Sclerosis (MS) holds an epigenetic component that mediates the effects of its typical environmental risk factors on disease progression. Some of the major epigenetic modifications on DNA are the addition of methyl or a hydroxymethyl group to the C5 cytosine position, leading to 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) synthesis. Interestingly, abnormal epigenetic modification patterns, such as the global DNA methylation loss in MS brain white matter, link to several neurodegenerative disorders. Abnormal DNA methylation/hydroxymethylation enzymes expression is also extensively documented in Alzheimer’s disease and cancer. This doctoral research project traces the DNA methylation instability in MS white matter, back to the altered expression of the DNA methylation/hydroxymethylation enzymes.

DNA Methylation changes in the brain white matter of multiple sclerosis patients

TAGLIATESTA, STEFANO
2020

Abstract

The literature implies that Multiple Sclerosis (MS) holds an epigenetic component that mediates the effects of its typical environmental risk factors on disease progression. Some of the major epigenetic modifications on DNA are the addition of methyl or a hydroxymethyl group to the C5 cytosine position, leading to 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) synthesis. Interestingly, abnormal epigenetic modification patterns, such as the global DNA methylation loss in MS brain white matter, link to several neurodegenerative disorders. Abnormal DNA methylation/hydroxymethylation enzymes expression is also extensively documented in Alzheimer’s disease and cancer. This doctoral research project traces the DNA methylation instability in MS white matter, back to the altered expression of the DNA methylation/hydroxymethylation enzymes.
20-feb-2020
Inglese
DNA Methylation Multiple Sclerosis TET2 IDAX 5mC 5hmC 5fC 5caC Epigenetics
ZAMPIERI, Michele
PIZZUTI, Antonio
Università degli Studi di Roma "La Sapienza"
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14242/99060
Il codice NBN di questa tesi è URN:NBN:IT:UNIROMA1-99060