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从头合成嘧啶的多酶蛋白 CAD 仅定位于细胞质,不会易位到细胞核。

The multienzymatic protein CAD leading the de novo biosynthesis of pyrimidines localizes exclusively in the cytoplasm and does not translocate to the nucleus.

机构信息

Genome Dynamics and Function Program, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2020;39(10-12):1320-1334. doi: 10.1080/15257770.2019.1706743. Epub 2020 Jan 30.

Abstract

CAD, the multienzymatic protein that initiates and controls the biosynthesis of pyrimidines, plays a major role in nucleotide homeostasis, cell growth and proliferation. Despite its interest as a potential antitumoral target, there is a lack of understanding on CAD's structure and functioning mechanisms. Although mainly identified as a cytosolic complex, different studies support the translocation of CAD into the nucleus, where it could have a yet undefined function. Here, we track the subcellular localization of CAD by using fluorescent chimeras, cell fractionation and immunoblotting with specific antibodies. Contradicting previous studies, we demonstrate that CAD is exclusively localized at the cytosol and discard a possible translocation to the nucleus.

摘要

CAD 是一种多酶蛋白,可启动并控制嘧啶的生物合成,在核苷酸动态平衡、细胞生长和增殖中发挥重要作用。尽管 CAD 作为潜在的抗肿瘤靶点具有重要意义,但人们对其结构和作用机制的了解仍有限。尽管 CAD 主要被鉴定为胞质复合物,但不同的研究支持 CAD 易位到核内,其在核内可能具有尚未明确的功能。在这里,我们使用荧光嵌合体、细胞分级分离和用特异性抗体进行免疫印迹来跟踪 CAD 的亚细胞定位。与之前的研究相反,我们证明 CAD 仅定位于细胞质,不存在向核内易位的可能。

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