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母亲肥胖会增加与衰老相关的卵母细胞染色体异常。

Maternal obesity enhances oocyte chromosome abnormalities associated with aging.

作者信息

Yun Yan, Wei Zijie, Hunter Neil

机构信息

Howard Hughes Medical Institute, University of California, Davis, Davis, CA, USA.

Department of Microbiology & Molecular Genetics, University of California, Davis, Davis, CA, USA.

出版信息

Chromosoma. 2019 Sep;128(3):413-421. doi: 10.1007/s00412-019-00716-6. Epub 2019 Jul 8.

Abstract

Obesity is increasing globally, and maternal obesity has adverse effects on pregnancy outcomes and the long-term health of offspring. Maternal obesity has been associated with pregnancy failure through impaired oogenesis and embryogenesis. However, whether maternal obesity causes chromosome abnormalities in oocytes has remained unclear. Here we show that chromosome abnormalities are increased in the oocytes of obese mice fed a high-fat diet and identify weakened sister-chromatid cohesion as the likely cause. Numbers of full-grown follicles retrieved from obese mice were the same as controls and the efficiency of in vitro oocyte maturation remained high. However, chromosome abnormalities presenting in both metaphase-I and metaphase-II were elevated, most prominently the premature separation of sister chromatids. Weakened sister-chromatid cohesion in oocytes from obese mice was manifested both as the terminalization of chiasmata in metaphase-I and as increased separation of sister centromeres in metaphase II. Obesity-associated abnormalities were elevated in older mice implying that maternal obesity exacerbates the deterioration of cohesion seen with advancing age.

摘要

肥胖在全球范围内呈上升趋势,母体肥胖会对妊娠结局和后代的长期健康产生不利影响。母体肥胖通过损害卵子发生和胚胎发生与妊娠失败有关。然而,母体肥胖是否会导致卵母细胞染色体异常仍不清楚。在这里,我们表明,喂食高脂肪饮食的肥胖小鼠的卵母细胞中染色体异常增加,并确定姐妹染色单体黏连减弱是可能的原因。从肥胖小鼠中回收的成熟卵泡数量与对照组相同,体外卵母细胞成熟效率仍然很高。然而,在减数第一次分裂中期和减数第二次分裂中期出现的染色体异常均有所增加,最明显的是姐妹染色单体过早分离。肥胖小鼠卵母细胞中姐妹染色单体黏连减弱表现为减数第一次分裂中期交叉端化和减数第二次分裂中期姐妹着丝粒分离增加。老年小鼠中与肥胖相关的异常情况增加,这意味着母体肥胖会加剧随着年龄增长而出现的黏连恶化。

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