Immunology Programme, The Babraham Institute,Babraham Research Campus, Cambridge, United Kingdom.
RNA Biology Laboratory, Center for Cancer Research, National Cancer Institute (NCI), Frederick, United States.
Elife. 2022 Apr 22;11:e72313. doi: 10.7554/eLife.72313.
To identify roles of RNA binding proteins (RBPs) in the differentiation or survival of antibody secreting plasma cells we performed a CRISPR/Cas9 knockout screen of 1213 mouse RBPs for their ability to affect proliferation and/or survival, and the abundance of differentiated CD138 + cells in vitro. We validated the binding partners CSDE1 and STRAP as well as the mA binding protein YTHDF2 as promoting the accumulation of CD138 + cells in vitro. We validated the EIF3 subunits EIF3K and EIF3L and components of the CCR4-NOT complex as inhibitors of CD138 + cell accumulation in vitro. In chimeric mouse models YTHDF2-deficient plasma cells failed to accumulate.
为了确定 RNA 结合蛋白(RBPs)在分泌抗体的浆细胞分化或存活中的作用,我们对 1213 种小鼠 RBPs 进行了 CRISPR/Cas9 敲除筛选,以研究它们影响增殖和/或存活的能力,以及体外分化的 CD138+细胞的丰度。我们验证了结合伴侣 CSDE1 和 STRAP 以及 mA 结合蛋白 YTHDF2 可促进体外 CD138+细胞的积累。我们验证了 EIF3 亚基 EIF3K 和 EIF3L 以及 CCR4-NOT 复合物的成分是体外抑制 CD138+细胞积累的抑制剂。在嵌合小鼠模型中,YTHDF2 缺陷型浆细胞未能积累。