Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Tytuł pozycji:

Methylation status of CpG sites in the NOTCH4 promoter region regulates NOTCH4 expression in patients with tetralogy of Fallot.

Tytuł:
Methylation status of CpG sites in the NOTCH4 promoter region regulates NOTCH4 expression in patients with tetralogy of Fallot.
Autorzy:
Zhu Y; Institute of Paediatrics, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.
Ye M; Cardiovascular Centre, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.
Xu H; Department of Forensic Medicine, Soochow University, Suzhou, Jiangsu 215006, P.R. China.
Gu R; Cardiovascular Centre, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.
Ma X; Cardiovascular Centre, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.
Chen M; Division of Life Sciences and Medicine, The First Affiliated Hospital of The University of Science and Technology of China, Hefei, Anhui 230036, P.R. China.
Li X; Institute of Paediatrics, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.
Sheng W; Institute of Paediatrics, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.
Huang G; Institute of Paediatrics, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.
Źródło:
Molecular medicine reports [Mol Med Rep] 2020 Nov; Vol. 22 (5), pp. 4412-4422. Date of Electronic Publication: 2020 Sep 24.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Athens, Greece : D. A. Spandidos
MeSH Terms:
DNA Methylation*
Down-Regulation*
Receptor, Notch4/*genetics
Receptor, Notch4/*metabolism
Tetralogy of Fallot/*genetics
Adolescent ; Case-Control Studies ; Child ; Child, Preschool ; CpG Islands ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Promoter Regions, Genetic ; Proto-Oncogene Protein c-ets-1/metabolism ; Sequence Analysis, DNA ; Tetralogy of Fallot/metabolism
References:
Circulation. 2007 Jun 12;115(23):3015-38. (PMID: 17519398)
Nat Genet. 2009 Feb;41(2):178-186. (PMID: 19151715)
Proc Natl Acad Sci U S A. 2001 May 8;98(10):5643-8. (PMID: 11344305)
Neuropsychopharmacology. 2018 Jan;43(2):342-353. (PMID: 28540928)
J Am Coll Cardiol. 2011 Nov 15;58(21):2241-7. (PMID: 22078432)
Cardiovasc Pathol. 2008 Jan-Feb;17(1):48-54. (PMID: 18160060)
Science. 1999 Apr 30;284(5415):770-6. (PMID: 10221902)
Hum Mol Genet. 2010 Feb 15;19(4):648-56. (PMID: 19942620)
Am J Med Genet A. 2013 Dec;161A(12):3133-6. (PMID: 23956173)
Nat Genet. 2010 Dec;42(12):1093-100. (PMID: 21057502)
J Steroid Biochem Mol Biol. 2012 May;130(1-2):96-104. (PMID: 22342840)
Circ Res. 2016 Jan 8;118(1):e1-e18. (PMID: 26635389)
Circ Res. 2011 Jul 8;109(2):183-92. (PMID: 21597012)
Lancet. 2014 Aug 30;384(9945):747-54. (PMID: 24768155)
Circ Res. 2015 Feb 13;116(4):700-14. (PMID: 25677518)
Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7588-92. (PMID: 7689222)
Mol Cell Biol. 2002 Apr;22(8):2830-41. (PMID: 11909975)
Science. 2001 Aug 10;293(5532):1068-70. (PMID: 11498573)
J Am Coll Cardiol. 2009 Nov 10;54(20):1883-90. (PMID: 19892240)
Cell. 1991 Mar 22;64(6):1123-34. (PMID: 2004419)
Oncogene. 2000 Feb 10;19(6):745-53. (PMID: 10698492)
Nat Biotechnol. 2010 Oct;28(10):1057-68. (PMID: 20944598)
Circulation. 2003 May 20;107(19):2467-74. (PMID: 12742993)
J Am Heart Assoc. 2014 Jun 19;3(3):e000976. (PMID: 24947998)
Arterioscler Thromb Vasc Biol. 2003 Apr 1;23(4):543-53. (PMID: 12615665)
Curr Mol Med. 2007 Feb;7(1):85-102. (PMID: 17311535)
Heart. 2001 Dec;86 Suppl 2:II3-11. (PMID: 11709529)
Development. 2002 Feb;129(4):1075-82. (PMID: 11861489)
N Engl J Med. 2018 Apr 05;378(14):1323-1334. (PMID: 29617578)
Ann Epidemiol. 2016 Dec;26(12):838-845. (PMID: 27894567)
J Clin Oncol. 2012 Jul 10;30(20):2483-91. (PMID: 22564988)
Genome Res. 2013 Jun;23(6):988-97. (PMID: 23590861)
J Steroid Biochem Mol Biol. 2017 Jul;171:209-217. (PMID: 28412323)
BMC Med Genomics. 2012 Jun 06;5:20. (PMID: 22672592)
Circ Res. 2019 Feb 15;124(4):553-563. (PMID: 30582441)
Mech Dev. 2001 Oct;108(1-2):161-4. (PMID: 11578869)
BMC Med Genomics. 2019 May 28;12(1):75. (PMID: 31138201)
Genes Dev. 2000 Jun 1;14(11):1343-52. (PMID: 10837027)
Environ Int. 2017 Nov;108:127-136. (PMID: 28843141)
PLoS One. 2011;6(10):e25884. (PMID: 21991380)
BMC Med Genomics. 2013 Nov 01;6:46. (PMID: 24182332)
Clin Genet. 2019 Jan;95(1):85-94. (PMID: 29767458)
Environ Health Perspect. 2015 Aug;123(8):759-65. (PMID: 25769179)
Gene. 2003 Jan 16;303:11-34. (PMID: 12559563)
Dev Cell. 2013 Jul 15;26(1):45-58. (PMID: 23830865)
Immunity. 2012 Jun 29;36(6):921-32. (PMID: 22608498)
Dev Biol. 2007 Mar 15;303(2):772-83. (PMID: 17125762)
Development. 2010 May;137(9):1543-51. (PMID: 20356956)
J Allergy Clin Immunol. 2016 Mar;137(3):797-805.e5. (PMID: 26684294)
J Biol Chem. 2011 Aug 5;286(31):27092-102. (PMID: 21659508)
Circ Res. 2004 Apr 16;94(7):910-7. (PMID: 14988227)
Pediatr Res. 2016 Jul;80(1):151-8. (PMID: 26959486)
Cell. 2012 Nov 21;151(5):1083-96. (PMID: 23178125)
Substance Nomenclature:
0 (ETS1 protein, human)
0 (NOTCH4 protein, human)
0 (Proto-Oncogene Protein c-ets-1)
0 (Receptor, Notch4)
Entry Date(s):
Date Created: 20201001 Date Completed: 20210430 Latest Revision: 20210430
Update Code:
20240105
PubMed Central ID:
PMC7533461
DOI:
10.3892/mmr.2020.11535
PMID:
33000281
Czasopismo naukowe
Tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease (CHD). Although a lower methylation level of whole genome has been demonstrated in TOF patients, little is known regarding the DNA methylation changes in specific gene and its associations with TOF development. NOTCH4 is a mediator of the Notch signalling pathway that plays an important role in normal cardiac development. However, the role of epigenetic regulation of the NOTCH4 gene in the pathogenesis of TOF remains unclear. Considering the NOTCH4 low mutation frequency and reduced expression in the TOF patients, we hypothesized that abnormal DNA methylation change of NOTCH4 gene may influence its expression and responsible for TOF development. In this study, we measured the promoter methylation status of NOTCH4 and was measured and its regulation mechanism was explored, which may be related to TOF disease. Additionally, the promoter methylation statuses of NOTCH4 was measured in order to further understand epigenetic mechanisms that may serve a role in the development of TOF. Immunohistochemical analysis was used to examine NOTCH4 expression in right ventricular outflow tract myocardial tissues in patients with TOF. Compared with healthy controls, patients with TOF displayed significantly reduced in NOTCH4 expression (P=0.0055). Moreover, bisulphite sequencing suggested that the methylation levels of CpG site 2 in the NOTCH4 promoter was significantly higher in the patients than in the controls (P=0.0459). NOTCH4 expression was negatively associated with CpG site 2 methylation levels (r=‑0.51; P=0.01). ETS1 transcription factor can serve as transcriptional activators by binding to specific DNA sequences of target genes, such as DLL4 and NOTCH4, which serves an important role in normal heart development. Dual‑luciferase reporter and electrophoretic mobility shift assays indicated that the ETS1 transcription factor could bind to the NOTCH4 promoter region. However, binding of ETS1 to the NOTCH4 promoter was abrogated by methylation at the putative ETS1 binding sites. These findings suggested that decreased NOTCH4 expression in patients with TOF may be associated with hypermethylation of CpG site 2 in the NOTCH4 promoter region, due to impaired binding of ETS1.
Zaloguj się, aby uzyskać dostęp do pełnego tekstu.

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies