DNA Methylation Developmental Programming and Cellular Memory: The Molecular Consequences of Folate Depletion In Utero

DNA 甲基化发育编程和细胞记忆:子宫内叶酸消耗的分子后果

基本信息

  • 批准号:
    BB/G007993/1
  • 负责人:
  • 金额:
    $ 63.72万
  • 依托单位:
  • 依托单位国家:
    英国
  • 项目类别:
    Research Grant
  • 财政年份:
    2009
  • 资助国家:
    英国
  • 起止时间:
    2009 至 无数据
  • 项目状态:
    已结题

项目摘要

Summary Poor maternal nutrition can have profound effects on the long-term health and wellbeing of offspring and may cause premature ageing. These adverse effects on health include common diseases such as obesity, type 2 diabetes and cardiovascular disease. The risk of these conditions appears to be exacerbated when the offspring gain weight more quickly than would have been expected. In preliminary studies, we observed that mice born to mothers given diets low in folate (a B vitamin) during pregnancy and lactation became heavier adults than those born to mothers with normal folate supply despite the fact that there were no differences in body weight between the two groups of mice at weaning and that all mice received the same diet from weaning. This suggests that the maternal nutritional insult was 'remembered' by the mouse tissues and expressed as more rapid growth. Change in epigenetic markings is one of the most important mechanisms believed to be responsible for cellular 'memorisation' of early life experiences. Epigenetics describes chemical changes to the genome which regulate when and where genes are expressed (turned on) but which do not alter the primary DNA sequence. The best understood of the epigenetic marks is DNA methylation i.e. the addition of CH3 (methyl) groups to DNA. In our mouse studies we found that there were fewer CH3 groups in the DNA from adult mice born to the folate-depleted mothers. In follow up studies we have found that maternal folate depletion resulted in altered expression of over 600 genes in fetal liver. In this project we will investigate in more detail the effects of low maternal folate supply on growth and body fatness of the offspring and we will examine the effects of feeding high v. low fat diets from weaning. We anticipate that the high fat diet (based on the composition of Western human diets) will exacerbate the effects of the maternal nutritional insult. We will use state-of-the-art magnetic resonance imaging to allow us to measure how much fat is in the live mice and in which parts of the body it is stored. In humans, fat stored in the abdomen is associated with higher risk of several common disease including type 2 diabetes, cardiovascular disease and bowel cancer. We will then explore the mechanisms responsible for these phenotypic changes. We will focus on identification of genes whose expression has been changed through altered epigenetic markings and attempt to elucidate the molecular events leading to the genes being switched off, or switched on, inappropriately.
母亲营养不良会对后代的长期健康和福祉产生深远影响,并可能导致过早衰老。这些对健康的不利影响包括常见疾病,如肥胖、2型糖尿病和心血管疾病。当后代体重增加的速度比预期的要快时,这些疾病的风险似乎会加剧。在初步研究中,我们观察到,在怀孕和哺乳期间给予低叶酸(一种B族维生素)饮食的母亲所生的小鼠比叶酸供应正常的母亲所生的小鼠成年后体重更重,尽管事实上两组小鼠在断奶时的体重没有差异,并且所有小鼠在断奶时接受相同的饮食。这表明母体营养损伤被小鼠组织“记住”,并表现为更快速的生长。表观遗传标记的变化被认为是负责细胞对早期生活经历的“记忆”的最重要机制之一。表观遗传学描述了基因组的化学变化,这些变化调节基因表达(打开)的时间和位置,但不改变主要的DNA序列。对表观遗传标记的最好理解是DNA甲基化,即向DNA添加CH3(甲基)基团。在我们的小鼠研究中,我们发现叶酸缺乏的母亲所生的成年小鼠的DNA中CH3基团较少。在后续研究中,我们发现母体叶酸耗尽导致胎儿肝脏中600多个基因的表达改变。在这个项目中,我们将更详细地调查低母体叶酸供应对后代生长和体脂肪的影响,我们将检查从断奶开始喂养高脂肪和低脂肪饮食的影响。我们预计,高脂肪饮食(基于西方人类饮食的组成)将加剧产妇营养损害的影响。我们将使用最先进的磁共振成像技术来测量活小鼠体内有多少脂肪以及脂肪储存在身体的哪些部位。在人类中,储存在腹部的脂肪与几种常见疾病的高风险有关,包括2型糖尿病,心血管疾病和肠癌。然后,我们将探讨这些表型变化的机制。我们将专注于识别基因的表达已被改变,通过改变表观遗传标记,并试图阐明导致基因被关闭或打开,不适当的分子事件。

项目成果

期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Genetic and non-genetic influences during pregnancy on infant global and site specific DNA methylation: role for folate gene variants and vitamin B12.
  • DOI:
    10.1371/journal.pone.0033290
  • 发表时间:
    2012
  • 期刊:
  • 影响因子:
    3.7
  • 作者:
    McKay JA;Groom A;Potter C;Coneyworth LJ;Ford D;Mathers JC;Relton CL
  • 通讯作者:
    Relton CL
Impact of In Utero Folate Exposure on DNA Methylation and Its Potential Relevance for Later-Life Health-Evidence from Mouse Models Translated to Human Cohorts.
  • DOI:
    10.1002/mnfr.202100789
  • 发表时间:
    2022-03
  • 期刊:
  • 影响因子:
    5.2
  • 作者:
    Kok DE;Richmond RC;Adriaens M;Evelo CT;Ford D;Mathers JC;Robinson N;McKay JA
  • 通讯作者:
    McKay JA
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John Mathers其他文献

OR25-07-23 Abbreviated Score To Assess Adherence to the 2018 WCRF/AICR Cancer Prevention Recommendations and Risk of Cancer in the UK Biobank Cohort
  • DOI:
    10.1016/j.cdnut.2023.100457
  • 发表时间:
    2023-07-01
  • 期刊:
  • 影响因子:
  • 作者:
    Fiona Malcomson;Solange Parra-Soto;Frederick Ho;Carlos Celis-Morales;Linda Sharp;John Mathers
  • 通讯作者:
    John Mathers
OR06-04-23 Objectively Measured Physical Activity and Risk of Colorectal Cancer: Evidence From the UK Biobank Cohort Study
  • DOI:
    10.1016/j.cdnut.2023.101761
  • 发表时间:
    2023-07-01
  • 期刊:
  • 影响因子:
  • 作者:
    Solange Parra-Soto;Fiona Malcomson;John Mathers;Frederick Ho;Katrina Knight;Jill Pell;Carlos Celis-Morales
  • 通讯作者:
    Carlos Celis-Morales
SAT146 - A meditarranean diet intervention has beneficial effects on biomarkers of cardiovascular risk and hepatic fibrosis in non-alcoholic fatty liver disease (NAFLD)
SAT146 - 地中海饮食干预对非酒精性脂肪肝疾病(NAFLD)中心血管风险和肝纤维化的生物标志物具有有益影响
  • DOI:
    10.1016/s0168-8278(22)01788-3
  • 发表时间:
    2022-07-01
  • 期刊:
  • 影响因子:
    33.000
  • 作者:
    Laura Haigh;Olivier Govaere;Lorna Brownlee;Sarah Charman;Alasdair Blain;Thomas Wilson;Morten Karsdal;Stuart Mcpherson;John Mathers;Quentin Anstee
  • 通讯作者:
    Quentin Anstee
P32. Buccal cells as a surrogate DNA source for methylation biomarkers to identify those at increased colorectal cancer risk
  • DOI:
    10.1016/j.ejso.2012.07.153
  • 发表时间:
    2012-11-01
  • 期刊:
  • 影响因子:
  • 作者:
    Helen Staley;David Bradburn;John Mathers
  • 通讯作者:
    John Mathers
SAT-254 Diet modifies the association between alcohol intake and alcohol-related liver disease: a prospective study of individual patient data from the UK Biobank
  • DOI:
    10.1016/s0168-8278(24)00701-3
  • 发表时间:
    2024-06-01
  • 期刊:
  • 影响因子:
  • 作者:
    Fanny Petermann;Ziyi Zhou;John Mathers;Carlos Celis-Morales;David Raubenheimer;Naveed Sattar;Jill Pell;Ewan H. Forrest;Frederick Ho
  • 通讯作者:
    Frederick Ho

John Mathers的其他文献

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{{ truncateString('John Mathers', 18)}}的其他基金

Development of interventions to enhance health and wellbeing in later life (The LIVEWELL programme)
制定干预措施以增强晚年的健康和福祉(LIVEWELL 计划)
  • 批准号:
    G0900686/1
  • 财政年份:
    2010
  • 资助金额:
    $ 63.72万
  • 项目类别:
    Research Grant
BBSRC DRINC Training Grant 2010
BBSRC DRINC 培训补助金 2010
  • 批准号:
    BB/H532067/1
  • 财政年份:
    2010
  • 资助金额:
    $ 63.72万
  • 项目类别:
    Training Grant
Impact of non-digestible carbohydrates on biomarkers of GI health: a human intervention study
不可消化的碳水化合物对胃肠道健康生物标志物的影响:一项人类干预研究
  • 批准号:
    BB/H005013/1
  • 财政年份:
    2010
  • 资助金额:
    $ 63.72万
  • 项目类别:
    Research Grant

相似海外基金

Postdoctoral Fellowship: SPRF: Early Life Adversity Effects on DNA Methylation: Developmental Trajectories and Functional Consequences
博士后奖学金:SPRF:早期生活逆境对 DNA 甲基化的影响:发育轨迹和功能后果
  • 批准号:
    2313953
  • 财政年份:
    2023
  • 资助金额:
    $ 63.72万
  • 项目类别:
    Fellowship Award
11/15/18. Bowers. Resub R01. Linking pre- and post-natal psychosocial determinants, DNA methylation, and early developmental health disparities
2018 年 11 月 15 日。
  • 批准号:
    10573269
  • 财政年份:
    2019
  • 资助金额:
    $ 63.72万
  • 项目类别:
11/15/18. Bowers. Resub R01. Linking pre- and post-natal psychosocial determinants, DNA methylation, and early developmental health disparities
2018 年 11 月 15 日。
  • 批准号:
    10339401
  • 财政年份:
    2019
  • 资助金额:
    $ 63.72万
  • 项目类别:
Developmental regulation of HBV biosynthesis by FoxA and DNA methylation
FoxA 和 DNA 甲基化对 HBV 生物合成的发育调控
  • 批准号:
    9906839
  • 财政年份:
    2016
  • 资助金额:
    $ 63.72万
  • 项目类别:
Developmental regulation of HBV biosynthesis by FoxA and DNA methylation
FoxA 和 DNA 甲基化对 HBV 生物合成的发育调控
  • 批准号:
    9275362
  • 财政年份:
    2016
  • 资助金额:
    $ 63.72万
  • 项目类别:
Developmental regulation of HBV biosynthesis by FoxA and DNA methylation
FoxA 和 DNA 甲基化对 HBV 生物合成的发育调控
  • 批准号:
    9156108
  • 财政年份:
    2016
  • 资助金额:
    $ 63.72万
  • 项目类别:
Sites of Developmental & Tissue-specific DNA Methylation
发育部位
  • 批准号:
    6891365
  • 财政年份:
    2004
  • 资助金额:
    $ 63.72万
  • 项目类别:
Sites of Developmental & Tissue-specific DNA Methylation
发育部位
  • 批准号:
    6778565
  • 财政年份:
    2004
  • 资助金额:
    $ 63.72万
  • 项目类别:
Sites of Developmental & Tissue-specific DNA Methylation
发育部位
  • 批准号:
    7225212
  • 财政年份:
    2004
  • 资助金额:
    $ 63.72万
  • 项目类别:
Sites of Developmental & Tissue-specific DNA Methylation
发育部位
  • 批准号:
    7065198
  • 财政年份:
    2004
  • 资助金额:
    $ 63.72万
  • 项目类别:
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