Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.
Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China. Electronic address: https://twitter.com/huabin_zhou.
J Mol Biol. 2021 Nov 5;433(22):167269. doi: 10.1016/j.jmb.2021.167269. Epub 2021 Sep 24.
VERNALIZATION1 (VRN1) is a transcriptional repressor involved in plant vernalization that undergoes liquid-liquid phase separation (LLPS) with DNA. The naturally occurring VRN1-like proteins contain two B3 DNA binding domains connected by an intrinsically disordered region (IDR). The IDR length in VRN1-like proteins has a broad distribution, while the charge segregation pattern is largely conserved. We studied the effect of IDR length and charge segregation on DNA-induced VRN1 phase separation. When only neutral residues (Pro-Ser repeats) were used, the phase separation behavior is sensitive to IDR length, changing from gel-like aggregates (L = 40) to liquid-like droplets (L = 100-120) and clear solution (L = 160). When a pair of continuous patches of positive and negative residues were added to the IDRs, all the VRN1 variants formed robust and durable droplets with DNA independent of the IDR length. To test how robust the system is, we introduced folded green fluorescent protein or the enzyme GPX4 into VRN1 variants with charge segregation in IDR, the resulting proteins form LLPS with DNA as well. Our study implies that VRN1-like proteins use conserved charge segregation pattern to retain functional LLPS during evolution, and demonstrates the possibility of using this system to design novel biosensors or bio-factories by introducing various functional modules.
春化(VRN1)是一种参与植物春化的转录抑制剂,它与 DNA 发生液-液相分离(LLPS)。天然存在的 VRN1 样蛋白包含两个通过无规卷曲区域(IDR)连接的 B3 DNA 结合结构域。VRN1 样蛋白的 IDR 长度分布广泛,而电荷分离模式则在很大程度上保持保守。我们研究了 IDR 长度和电荷分离对 DNA 诱导 VRN1 相分离的影响。当仅使用中性残基(脯氨酸-丝氨酸重复序列)时,相分离行为对 IDR 长度敏感,从凝胶状聚集体(L=40)变为液态液滴(L=100-120)和澄清溶液(L=160)。当在 IDR 中添加一对连续的正负残基补丁时,所有带有 DNA 的 VRN1 变体都形成了稳健且持久的液滴,与 IDR 长度无关。为了测试系统的稳健性,我们将折叠的绿色荧光蛋白或酶 GPX4 引入带有 IDR 中电荷分离的 VRN1 变体中,结果蛋白也与 DNA 形成 LLPS。我们的研究表明,VRN1 样蛋白在进化过程中利用保守的电荷分离模式保留功能性 LLPS,并证明了通过引入各种功能模块,利用该系统设计新型生物传感器或生物工厂的可能性。