DNA methylation changes in infants between 6 and 52 weeks

被引:19
作者
Wikenius, Ellen [1 ,2 ]
Moe, Vibeke [3 ,4 ]
Smith, Lars [3 ]
Heiervang, Einar R. [2 ,5 ]
Berglund, Anders [1 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
[2] Univ Oslo, Fac Med, Inst Clin Med, Oslo, Norway
[3] Univ Oslo, Fac Social Sci, Dept Psychol, Oslo, Norway
[4] Eastern & Southern Norway RBUP, Ctr Child & Adolescent Mental Hlth, Oslo, Norway
[5] Oslo Univ Hosp, Oslo, Norway
关键词
EPIGENOME-WIDE ASSOCIATION; TUMOR-SUPPRESSOR; EPIGENETIC DRIFT; HUMAN BRAIN; CANCER; IDENTIFICATION; GENE; EXPRESSION; TRANSCRIPTION; MEMBRANE;
D O I
10.1038/s41598-019-54355-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Infants undergo extensive developments during their first year of life. Although the biological mechanisms involved are not yet fully understood, changes in the DNA methylation in mammals are believed to play a key role. This study was designed to investigate changes in infant DNA methylation that occurs between 6 and 52 weeks. A total of 214 infant saliva samples from 6 or 52 weeks were assessed using principal component analyses and t-distributed stochastic neighbor-embedding algorithms. Between the two time points, there were clear differences in DNA methylation. To further investigate these findings, paired two-sided student's t-tests were performed. Differently methylated regions were defined as at least two consecutive probes that showed significant differences, with a q-value < 0.01 and a mean difference > 0.2. After correcting for false discovery rates, changes in the DNA methylation levels were found in 42 genes. Of these, 36 genes showed increased and six decreased DNA methylation. The overall DNA methylation changes indicated decreased gene expression. This was surprising because infants undergo such profound developments during their first year of life. The results were evaluated by taking into consideration the extensive development that occurs during pregnancy. During the first year of life, infants have an overall three-fold increase in weight, while the fetus develops from a single cell into a viable infant in 9 months, with an 875-million-fold increase in weight. It is possible that the findings represent a biological slowing mechanism in response to extensive fetal development. In conclusion, our study provides evidence of DNA methylation changes during the first year of life, representing a possible biological slowing mechanism. We encourage future studies of DNA methylation changes in infants to replicate the findings by using a repeated measures model and less stringent criteria to see if the same genes can be found, as well as investigating whether other genes are involved in development during this period.
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页数:12
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共 103 条
  • [1] Birth weight-for-gestational age is associated with DNA methylation at birth and in childhood
    Agha, Golareh
    Hajj, Hanine
    Rifas-Shiman, Sheryl L.
    Just, Allan C.
    Hivert, Marie-France
    Burris, Heather H.
    Lin, Xihong
    Litonjua, Augusto A.
    Oken, Emily
    DeMeo, Dawn L.
    Gillman, Matthew W.
    Baccarelli, Andrea A.
    [J]. CLINICAL EPIGENETICS, 2016, 8
  • [2] Meis2 is a Pax6 co-factor in neurogenesis and dopaminergic periglomerular fate specification in the adult olfactory bulb
    Agoston, Zsuzsa
    Heine, Peer
    Brill, Monika S.
    Grebbin, Britta Moyo
    Hau, Ann-Christin
    Kallenborn-Gerhardt, Wiebke
    Schramm, Jasmine
    Goetz, Magdalena
    Schulte, Dorothea
    [J]. DEVELOPMENT, 2014, 141 (01): : 28 - 38
  • [3] SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy
    Agrawal, Pankaj B.
    Pierson, Christopher R.
    Joshi, Mugdha
    Liu, Xiaoli
    Ravenscroft, Gianina
    Moghadaszadeh, Behzad
    Talabere, Tiffany
    Viola, Marissa
    Swanson, Lindsay C.
    Haliloglu, Goknur
    Talim, Beril
    Yau, Kyle S.
    Allcock, Richard J. N.
    Laing, Nigel G.
    Perrella, Mark A.
    Beggs, Alan H.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2014, 95 (02) : 218 - 226
  • [4] Epigenetic associations of type 2 diabetes and BMI in an Arab population
    Al Muftah, Wadha A.
    Al-Shafai, Mashael
    Zaghlool, Shaza B.
    Visconti, Alessia
    Tsai, Pei-Chien
    Kumar, Pankaj
    Spector, Tim
    Bell, Jordana
    Falchi, Mario
    Suhre, Karsten
    [J]. CLINICAL EPIGENETICS, 2016, 8
  • [5] Systematic Review and Meta-Analysis of Circulating S100B Blood Levels in Schizophrenia
    Aleksovska, Katina
    Leoncini, Emanuele
    Bonassi, Stefano
    Cesario, Alfredo
    Boccia, Stefania
    Frustaci, Alessandra
    [J]. PLOS ONE, 2014, 9 (09):
  • [6] Genome-wide DNA methylation profiling of recurrent and non-recurrent chordomas
    Alholle, A.
    Brini, A. T.
    Bauer, J.
    Gharanei, S.
    Niada, S.
    Slater, A.
    Gentle, D.
    Maher, E. R.
    Jeys, L.
    Grimer, R.
    Sumathi, V. P.
    Latif, F.
    [J]. EPIGENETICS, 2015, 10 (03) : 213 - 220
  • [7] [Anonymous], IMPROVED PREDICTION
  • [8] Systematic pan-cancer analysis of tumour purity
    Aran, Dvir
    Sirota, Marina
    Butte, Atul J.
    [J]. NATURE COMMUNICATIONS, 2015, 6
  • [9] Assenov Y, 2014, NAT METHODS, V11, P1138, DOI [10.1038/NMETH.3115, 10.1038/nmeth.3115]
  • [10] Transthyretin Blocks Retinol Uptake and Cell Signaling by the Holo-Retinol-Binding Protein Receptor STRA6
    Berry, Daniel C.
    Croniger, Colleen M.
    Ghyselinck, Norbert B.
    Noy, Noa
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2012, 32 (19) : 3851 - 3859