Infrequent occurrence of age-dependent changes in CpG island methylation as detected by restriction landmark genome scanning

2002 ◽  
Vol 123 (11) ◽  
pp. 1487-1503 ◽  
Author(s):  
John Tra ◽  
Tadashi Kondo ◽  
Qianjin Lu ◽  
Rork Kuick ◽  
Samir Hanash ◽  
...  
2021 ◽  
Vol 19 ◽  
Author(s):  
Tingting Pi ◽  
Guangping Lang ◽  
Bo Liu ◽  
Jingshan Shi

Background: High methionine-diet (HMD) causes Alzheimer's disease (AD)-like symptoms. Previous studies have shown that Dendrobium nobile Lindle. alkaloids (DNLA) had potential benefits for AD. Object: Whether DNLA can improve AD-like symptoms induced by HMD is to be explored. Method: Mice were fed with 2% HMD diet for 11 weeks, the DNLA20 control group (20 mg/kg), DNLA10 group (10 mg/kg), and DNLA20 group (20 mg/kg) were administrated with DNLA for 3 months. Morris water maze test was used to detect learning and memory ability. Neuron damage was evaluated by HE and Nissl stainings. Levels of homocysteine (Hcy), beta-amyloid 1-42 (Aβ1-42), S-adenosine methionine (SAM), and S-adenosine homocysteine (SAH) were detected by ELISA. Immunofluorescence and western blotting (WB) were used to determine the expression of proteins. CPG island methylation. Results: Morris water maze test revealed that DNLA improved learning and memory dysfunction. HE, Nissl, and immunofluorescence stainings showed that DNLA alleviated neuron damage and reduced the 5-methylcytosine (5-mC), Aβ1-40, and Aβ1-42 levels. DNLA also decreased the levels of Hcy and Aβ1-42 in the serum, along with decreased SAM/SAH levels in the liver tissue. WB results showed that DNLA down-regulated the expression of the amyloid-precursor protein (APP), presenilin-1 (PS1), beta-secretase-1 (BACE1), DNA methyltransferase1 (DNMT1), Aβ1-40, and Aβ1-42 proteins. DNLA also up-regulated the expression of the protein of insulin-degrading enzyme (IDE), neprilysin (NEP), DNMT3a, and DNMT3b. Meanwhile, DNLA increased CPG island methylation levels of APP and BACE1 genes. Conclusions: DNLA alleviated AD-like symptoms induced by HMD via the DNA methylation pathway.


2004 ◽  
Vol 67 (1/2) ◽  
pp. 159-165 ◽  
Author(s):  
M. Eva Alonso ◽  
M. Josefa Bello ◽  
Pilar Gonzalez-Gomez ◽  
Dolores Arjona ◽  
Jose M. de Campos ◽  
...  

2014 ◽  
Vol 8 (5) ◽  
pp. 2340-2344 ◽  
Author(s):  
YU SONG ◽  
YUN ZUO

2015 ◽  
Vol 7 (1) ◽  
Author(s):  
Scott M. Langevin ◽  
Melissa Eliot ◽  
Rondi A. Butler ◽  
Agnes Cheong ◽  
Xiang Zhang ◽  
...  

2009 ◽  
Vol 10 (1) ◽  
pp. 116 ◽  
Author(s):  
Christopher Previti ◽  
Oscar Harari ◽  
Igor Zwir ◽  
Coral del Val

2008 ◽  
Vol 69 (1) ◽  
pp. 282-291 ◽  
Author(s):  
Michael T. McCabe ◽  
Eva K. Lee ◽  
Paula M. Vertino

2005 ◽  
Vol 33 (4) ◽  
pp. 709-711 ◽  
Author(s):  
N.J. Belshaw ◽  
G.O. Elliott ◽  
E.A. Williams ◽  
J.C. Mathers ◽  
L. Buckley ◽  
...  

ESR1 is frequently silenced by CGI (CpG island) methylation, both in human colorectal tumours and, in an age-dependent manner, in healthy mucosa. It is not clear, however, whether methylation of individual cytosines occurs randomly within the epithelial genome, or preferentially within individual cells as an ‘all-or-nothing’ phenomenon. CGI methylation can be quantified in human DNA residues recovered from faecal samples. We used bisulphite genomic sequencing of human DNA from this source and from a colorectal cancer cell line (SW48) to show that the ESR1 CGI is methylated in an allele-specific manner. This provides support for the ‘all or none’ mechanism for methylation of this gene, and shows how age-dependent methylation of the ESR1 CGI leads rapidly to silencing of the gene within the cells, and hence the colonic crypt within which it occurs. Preliminary studies with a rodent model suggest the rate of age-dependent methylation of ESR1 is modifiable by dietary folate.


2009 ◽  
Vol 19 (3) ◽  
pp. 146-155 ◽  
Author(s):  
Carmen S. Tellez ◽  
Lanlan Shen ◽  
Marcos R.H. Estécio ◽  
Jaroslav Jelinek ◽  
Jeffrey E. Gershenwald ◽  
...  

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