Center of Reproduction and Genetics, Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, China.
Central Laboratory, Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, China.
J Cell Physiol. 2018 Sep;233(9):7055-7066. doi: 10.1002/jcp.26507. Epub 2018 Mar 25.
The N6-methyladenosine (m6A) modification plays a central role in epigenetic regulation of the mammalian transcriptome. m6A can be demethylated by the fat mass- and obesity-associated (FTO) protein and the α-ketoglutarate-dependent dioxygenase alkB homolog 5 (ALKBH5) protein. Much less is known about that whether m6A content is involved in POI (premature ovarian insufficiency) disease. In this case-controlled study, 69 POI and 53 tubal occlusion patients were recruited from the reproduction centers in our hospital. For the POI animal model experiment, ovarian tissue was obtained from ten POI and nine healthy mice. An m6A test kit was developed to determine the m6A content in the RNA, and qPCR and western blot were used to examine the mRNA and protein expression levels of FTO and ALKBH5. FACS was used to measure the levels of proliferation and apoptosis, and siRNA was used to establish FTO and ALKBH5 knockdown cell lines. Our results showed that the m6A content in the RNA from POI patients and POI mice was significantly higher than control groups and that POI was characterized by the content of m6A. The mRNA and protein expression levels of FTO were significantly lower in the POI patients than control group and were associated with a risk of POI. These data suggest that the decreased mRNA and protein expression levels of FTO may be responsible for the increase in m6A in POI, which may further increase the risk of complications of POI. High m6A should be investigated further as a novel potential biomarker of POI.
N6-甲基腺苷(m6A)修饰在哺乳动物转录组的表观遗传调控中发挥核心作用。m6A 可以被脂肪量和肥胖相关(FTO)蛋白和 α-酮戊二酸依赖性双加氧酶 alkB 同源物 5(ALKBH5)蛋白去甲基化。关于 m6A 含量是否参与 POI(卵巢早衰)疾病知之甚少。在这项病例对照研究中,从我院生殖中心招募了 69 名 POI 和 53 名输卵管阻塞患者。对于 POI 动物模型实验,从 10 名 POI 和 9 名健康小鼠中获得卵巢组织。开发了 m6A 测试试剂盒来确定 RNA 中的 m6A 含量,并使用 qPCR 和 Western blot 检测 FTO 和 ALKBH5 的 mRNA 和蛋白表达水平。FACS 用于测量增殖和凋亡水平,并用 siRNA 建立 FTO 和 ALKBH5 敲低细胞系。我们的结果表明,POI 患者和 POI 小鼠的 RNA 中的 m6A 含量明显高于对照组,并且 POI 的特征是 m6A 的含量。POI 患者的 FTO mRNA 和蛋白表达水平明显低于对照组,与 POI 的风险相关。这些数据表明,FTO 的 mRNA 和蛋白表达水平降低可能导致 POI 中 m6A 的增加,这可能进一步增加 POI 并发症的风险。高 m6A 应进一步研究,作为 POI 的一种新的潜在生物标志物。
J Cell Physiol. 2018-3-25
J Coll Physicians Surg Pak. 2022-9
Cell Death Dis. 2021-7-27
Proc Natl Acad Sci U S A. 2020-9-28
Genes (Basel). 2025-6-30
Front Endocrinol (Lausanne). 2025-5-30
Front Immunol. 2025-4-28
Reprod Sci. 2025-5-8
J Ovarian Res. 2025-4-30
Cell Death Discov. 2025-2-4
J Assist Reprod Genet. 2025-2