Shin Heegwon, Lee Jungmin, Kim Youngmi, Jang Seonghui, Ohn Takbum, Lee Younghoon
Department of Chemistry, KAIST, Daejeon 34141, Korea.
Department of Cellular and Molecular Medicine, Chosun University School of Medicine, Gwangju 61452, Korea.
BMB Rep. 2017 Jun;50(6):318-322. doi: 10.5483/bmbrep.2017.50.6.217.
Brain cytoplasmic 200 RNA (BC200 RNA) is a neuron-specific non-coding RNA, implicated in the inhibition of local synaptodendritic protein synthesis, and is highly expressed in some cancer cells. Although BC200 RNA has been shown to inhibit translation in vitro, the cellular location of this inhibition is unknown. In this study, we used a BC200 RNA-recognizing antibody to identify the cellular locations of BC200 RNA in HeLa cervical carcinoma cells. We observed punctate signals in both the cytoplasm and nucleus, and further discovered that BC200 RNA co-localized with the p-body decapping enzyme, DCP1A, and the heterogeneous nuclear ribonucleoprotein E2 (hnRNP E2). The latter is a known BC200 RNA-binding partner protein and a constituent of p-bodies. This suggests that BC200 RNA is localized to p-bodies via hnRNP E2. [BMB Reports 2017; 50(6): 318-322].
脑细胞质200 RNA(BC200 RNA)是一种神经元特异性非编码RNA,与局部突触树突蛋白合成的抑制有关,且在某些癌细胞中高度表达。尽管BC200 RNA已被证明在体外可抑制翻译,但其抑制作用的细胞定位尚不清楚。在本研究中,我们使用一种识别BC200 RNA的抗体来鉴定HeLa宫颈癌细胞中BC200 RNA的细胞定位。我们在细胞质和细胞核中均观察到点状信号,并进一步发现BC200 RNA与P小体去帽酶DCP1A以及不均一核核糖核蛋白E2(hnRNP E2)共定位。后者是一种已知的BC200 RNA结合伴侣蛋白,也是P小体的组成成分。这表明BC200 RNA通过hnRNP E2定位于P小体。[《BMB报告》2017年;50(6): 318 - 322]