Variation in DNA methylation in the KvDMR1 (ICR2) region in first-trimester human pregnancies

被引:4
作者
Miranda Furtado, Cristiana Libardi [1 ,2 ,3 ]
Salomao, Karina Bezerra [1 ]
Verruma, Carolina Gennari [1 ]
Paulino Leite, Sarah Blima [1 ]
Lopes Rios, Alvaro Fabricio [4 ]
Bialecka, Monika [2 ]
Moustakas, Ioannis [2 ,5 ]
Mei, Hailiang [5 ]
Paro de Paz, Claudia Cristina [1 ,6 ]
Duarte, Geraldo [3 ]
Lopes, Susana M. Chuva de Sousa [2 ]
Ramos, Ester Silveira [1 ]
机构
[1] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Genet, Sao Paulo, Brazil
[2] Leiden Univ, Med Ctr, Dept Anat & Embryol, Leiden, Netherlands
[3] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Gynecol & Obstet, Sao Paulo, Brazil
[4] State Univ North Fluminense Darcy Ribeiro, Ctr Biosci & Biotechnol, Biotechnol Lab, Campos Dos Goytacazes, RJ, Brazil
[5] Leiden Univ, Med Ctr, Dept Biomed Data Sci, Sequencing Anal Support Core, Leiden, Netherlands
[6] Ctr APTA Bovinos Corte, Inst Zootecnia, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Bisulfite sequencing; DNA methylation; KvDMR1; pregnancy; real-time qPCR; BECKWITH-WIEDEMANN-SYNDROME; IMPRINTING CONTROL REGION; QUANTITATIVE-ANALYSIS; GENES; EXPRESSION; GROWTH; CHILD;
D O I
10.1016/j.fertnstert.2019.01.036
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To investigate the levels of DNA methylation in the KvDMR1 (KvLQT1 differentially methylated region 1) in embryonic and extra-embryonic tissues. Design: Cross-sectional study. Setting: University medical center and clinical hospital. Patient(s): Embryonic and/or extraembryonic tissues (umbilical cord, chorionic villus, chorion, decidua, and/or amnion) collected from 27 first-trimester pregnancies (up to 12 weeks of gestation, single embryos) from elective abortions, extravillous trophoblasts (EVTs) from the top of individual chorionic villi, and chorionic villi from 10 normal full-term placentas collected after birth. Intervention(s): None. Main Outcome Measure(s): DNA methylation of the KvDMR1 region evaluated using quantitative analysis of DNA methylation followed by real-time polymerase chain reaction (qAMP) and bisulfite sequencing (bis-seq) analysis. Result(s): The results showed variability in KvDMR1 DNA methylation in different tissues from the same pregnancy. The average of DNA methylation was not different between the embryo, umbilical cord, amnion, and chorionic villi, despite the relatively low level of methylation observed in the amnion (33.50% +/- 14.48%). Chorionic villi from term placentas showed a normal methylation pattern at KvDMR1 (42.60% +/- 6.08%). The normal methylation pattern at KvDMR1 in chorionic villi (as well as in EVTs) from first-trimester placentas was confirmed by bis-seq. Conclusion(s): Our results highlight an existing heterogeneity in DNA methylation of the KvDMR1 region during first trimester and a consistent hypomethylation in the amnion in this period of gestation. (Copyright (C) 2019 American Society for Reproductive Medicine, Published by Elsevier Inc.)
引用
收藏
页码:1186 / 1193
页数:8
相关论文
共 33 条
  • [1] Evolution of the CDKN1C-KCNQ1 imprinted domain
    Ager, Eleanor I.
    Pask, Andrew J.
    Gehring, Helen M.
    Shaw, Geoff
    Renfree, Marilyn B.
    [J]. BMC EVOLUTIONARY BIOLOGY, 2008, 8 (1)
  • [2] FETAL ORIGINS OF CORONARY HEART-DISEASE
    BARKER, DJP
    [J]. BRITISH MEDICAL JOURNAL, 1995, 311 (6998) : 171 - 174
  • [3] Detailed analysis of the methylation patterns of the KvDMR1 imprinting control region of human chromosome 11
    Beatty, L
    Weksberg, R
    Sadowski, PD
    [J]. GENOMICS, 2006, 87 (01) : 46 - 56
  • [4] Unearthing the Roles of Imprinted Genes in the Placenta
    Bressan, F. F.
    De Bem, T. H. C.
    Perecin, F.
    Lopes, F. L.
    Ambrosio, C. E.
    Meirelles, F. V.
    Miglino, M. A.
    [J]. PLACENTA, 2009, 30 (10) : 823 - 834
  • [5] Adaptations in placental phenotype support fetal growth during undernutrition of pregnant mice
    Coan, P. M.
    Vaughan, O. R.
    Sekita, Y.
    Finn, S. L.
    Burton, G. J.
    Constancia, M.
    Fowden, A. L.
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2010, 588 (03): : 527 - 538
  • [6] Beckwith-Wiedemann syndrome: Historical, clinicopathological, and etiopathogenetic perspectives
    Cohen, MM
    [J]. PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2005, 8 (03) : 287 - 304
  • [7] Imprinting evolution and human health
    Das, Radhika
    Hampton, Daniel D.
    Jirtle, Randy L.
    [J]. MAMMALIAN GENOME, 2009, 20 (9-10) : 563 - 572
  • [8] Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome
    Diaz-Meyer, N
    Day, CD
    Khatod, K
    Maher, ER
    Cooper, W
    Reik, W
    Junien, C
    Graham, G
    Algar, E
    Kaloustian, VMD
    Higgins, MJ
    [J]. JOURNAL OF MEDICAL GENETICS, 2003, 40 (11): : 797 - 801
  • [9] Differential expression of imprinted genes in normal and IUGR human placentas
    Diplas, Andreas I.
    Lambertini, Luca
    Lee, Men-Jean
    Sperling, Rhoda
    Lee, Yin Leng
    Wetmur, James
    Chen, Jia
    [J]. EPIGENETICS, 2009, 4 (04) : 235 - 240
  • [10] Methylation pattern at the KvDMR in a child with Beckwith-Wiedemann syndrome conceived by ICSI
    Gomes, M. V.
    Gomes, C. C.
    Pinto, W., Jr.
    Ramos, E. S.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2007, 143A (06) : 625 - 629