Chou Tsung-Wei, Huang Ing-Jen, Hsu Ya-Chu, Wu Szu-Hua, Hong Jui-Chung, Ko Yu-Hao, Su Ting-Ran, Jiang Jie-Hong Roland, Huang Hsiao-Chun
Institute of Molecular and Cellular Biology, National Taiwan University, Taipei, Taiwan.
Graduate Institute of Electronics Engineering, National Taiwan University, Taipei, Taiwan.
Commun Biol. 2025 Jul 20;8(1):1078. doi: 10.1038/s42003-025-08495-w.
Macromolecular complexes anchored at one cell pole have previously been utilized to achieve synthetic asymmetric cell division in Escherichia coli. In nature, however, robust asymmetric cell division often relies on gradients established between two opposing poles. Here, we present a second-generation synthetic genetic circuit that enables two distinct scaffolding proteins to localize at opposite poles in E. coli. By engineering a PodJ fragment as the second scaffold and integrating SpmX, a negative regulator of PodJ condensation, as a direct chimera with PopZ, we effectively confined PopZ and PodJ to opposite poles within E. coli. Additionally, we developed a neural network-based classification method to identify these synthetic dual-pole cells, further advancing the synthetic biology toolkit for programmable cell differentiation.
此前,锚定在一个细胞极的大分子复合物已被用于在大肠杆菌中实现合成不对称细胞分裂。然而,在自然界中,强大的不对称细胞分裂通常依赖于两个相对极之间建立的梯度。在这里,我们展示了一个第二代合成遗传电路,它能使两种不同的支架蛋白定位于大肠杆菌的相对极。通过设计一个PodJ片段作为第二个支架,并将PodJ凝聚的负调节因子SpmX作为与PopZ的直接嵌合体整合,我们有效地将PopZ和PodJ限制在大肠杆菌内的相对极。此外,我们开发了一种基于神经网络的分类方法来识别这些合成双极细胞,进一步推进了用于可编程细胞分化的合成生物学工具包。