Standaert Laura, Adriaens Carmen, Radaelli Enrico, Van Keymeulen Alexandra, Blanpain Cedric, Hirose Tetsuro, Nakagawa Shinichi, Marine Jean-Christophe
Center for the Biology of Disease, Laboratory for Molecular Cancer Biology, VIB, Leuven 3000, Belgium Center for Human Genetics, Laboratory for Molecular Cancer Biology, KULeuven, Leuven 3000, Belgium.
Center for the Biology of Disease, Histopathology Lab, VIB, Leuven 3000, Belgium Center for Human Genetics, Histopathology Lab, KULeuven, Leuven 3000, Belgium.
RNA. 2014 Dec;20(12):1844-9. doi: 10.1261/rna.047332.114. Epub 2014 Oct 14.
The lncRNA Neat1 is an essential architectural component of paraspeckle nuclear bodies. Although cell-based studies identified Neat1-paraspeckles as key regulators of gene expression through retention of hyperdited mRNAs and/or transcription factors, it is unclear under which specific physiological conditions paraspeckles are formed in vivo and whether they have any biological relevance. Herein, we show that paraspeckles are assembled in luminal epithelial cells during mammary gland development. Importantly, genetic ablation of Neat1 results in aberrant mammary gland morphogenesis and lactation defects. We provide evidence that the lactation defect is caused by a decreased ability of Neat1-mutant cells to sustain high rates of proliferation during lobular-alveolar development. This study is the first to assign an important biological function to the lncRNA Neat1 and to link it to the presence of paraspeckles nuclear bodies in vivo.
长链非编码RNA Neat1是旁斑核体的重要结构组成部分。尽管基于细胞的研究将Neat1旁斑确定为基因表达的关键调节因子,通过保留超编辑的mRNA和/或转录因子来实现,但尚不清楚在体内哪些特定生理条件下会形成旁斑,以及它们是否具有任何生物学意义。在此,我们表明旁斑在乳腺发育过程中的腔上皮细胞中组装。重要的是,Neat1的基因敲除导致乳腺形态发生异常和泌乳缺陷。我们提供证据表明,泌乳缺陷是由Neat1突变细胞在小叶-腺泡发育过程中维持高增殖率的能力下降所致。本研究首次赋予长链非编码RNA Neat1重要的生物学功能,并将其与体内旁斑核体的存在联系起来。