Arginine methylation-dependent METTL14-SMN interaction regulates RNA m6A homeostasis.

IF 6.2 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yi Zhang, Lei Shen, Lili Ren, Jiangbo Wei, Hoang Quoc Hai Pham, Xiaoqun Tao, Jiamin Guo, Zhihao Wang, Binghui Shen, Rui Su, Chuan He, Yanzhong Yang
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引用次数: 0

Abstract

N6-methyladenosine (m6A) homeostasis is essential for development, and its dysregulation is linked to cancers and neurological disorders. However, the mechanisms regulating m6A remain unclear. Here, we identify the survival of motoneuron (SMN) protein as a novel interaction partner of METTL14, a key component of the m6A methyltransferase complex. SMN binds METTL14 via its Tudor domain in an arginine methylation-dependent manner. Mutations in the SMN Tudor domain identified in spinal muscular atrophy (SMA) disrupt its interaction with METTL14 and reduce m6A levels in patient-derived fibroblasts, linking m6A dysregulation to SMA pathology. Both SMN knockdown and SMA mutations impair m6A deposition on the mRNAs of DNA repair genes, mirroring the effects of METTL14 hypomethylation. Consequently, SMA patient fibroblasts are hypersensitive to DNA-damaging agents due to reduced levels of DNA repair gene expression. To explore the function of METTL14 arginine methylation in vivo, we generated a Mettl14 methylation-deficient mouse model (Mettl14RK). Although this model does not show SMA-like phenotypes, the mutants are partially embryonic lethal and show abnormal hematopoiesis, underscoring a role for methylated METTL14 in early development.

精氨酸甲基化依赖的METTL14-SMN相互作用调节RNA m6A稳态。
n6 -甲基腺苷(m6A)体内平衡对发育至关重要,其失调与癌症和神经系统疾病有关。然而,调控m6A的机制仍不清楚。在这里,我们发现运动神经元(SMN)蛋白的存活是m6A甲基转移酶复合体的关键成分METTL14的一个新的相互作用伙伴。SMN通过其Tudor结构域以精氨酸甲基化依赖的方式结合METTL14。在脊髓性肌萎缩症(SMA)中发现的SMN Tudor结构域突变破坏了其与METTL14的相互作用,降低了患者源性成纤维细胞中m6A的水平,将m6A失调与SMA病理联系起来。SMN敲低和SMA突变都损害了m6A在DNA修复基因mrna上的沉积,反映了METTL14低甲基化的影响。因此,由于DNA修复基因表达水平降低,SMA患者成纤维细胞对DNA损伤剂过敏。为了探索METTL14精氨酸甲基化在体内的功能,我们建立了METTL14甲基化缺陷小鼠模型(Mettl14RK)。尽管该模型未显示sma样表型,但突变体部分胚胎致死性,并表现出异常的造血功能,强调甲基化的METTL14在早期发育中的作用。
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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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