School of Biological Science and Technology, College of Science and Engineering, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192, Japan.
National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, 411-8540, Japan.
Nat Commun. 2022 Mar 29;13(1):1660. doi: 10.1038/s41467-022-29316-2.
How cell size and number are determined during organ development remains a fundamental question in cell biology. Here, we identified a GRAS family transcription factor, called SCARECROW-LIKE28 (SCL28), with a critical role in determining cell size in Arabidopsis. SCL28 is part of a transcriptional regulatory network downstream of the central MYB3Rs that regulate G2 to M phase cell cycle transition. We show that SCL28 forms a dimer with the AP2-type transcription factor, AtSMOS1, which defines the specificity for promoter binding and directly activates transcription of a specific set of SIAMESE-RELATED (SMR) family genes, encoding plant-specific inhibitors of cyclin-dependent kinases and thus inhibiting cell cycle progression at G2 and promoting the onset of endoreplication. Through this dose-dependent regulation of SMR transcription, SCL28 quantitatively sets the balance between cell size and number without dramatically changing final organ size. We propose that this hierarchical transcriptional network constitutes a cell cycle regulatory mechanism that allows to adjust cell size and number to attain robust organ growth.
细胞大小和数量如何在器官发育过程中确定仍然是细胞生物学中的一个基本问题。在这里,我们鉴定了一个GRAS 家族转录因子,称为 SCARECROW-LIKE28(SCL28),它在拟南芥中决定细胞大小方面起着关键作用。SCL28 是调控 G2 到 M 期细胞周期转换的中央 MYB3Rs 的下游转录调控网络的一部分。我们表明,SCL28 与 AP2 型转录因子 AtSMOS1 形成二聚体,该二聚体决定启动子结合的特异性,并直接激活一组特定的 SIAMESE-RELATED(SMR)家族基因的转录,这些基因编码植物特异性细胞周期蛋白依赖性激酶抑制剂,从而抑制 G2 期的细胞周期进程,并促进内复制的开始。通过 SMR 转录的这种剂量依赖性调节,SCL28 在不显著改变最终器官大小的情况下,定量地调节细胞大小和数量之间的平衡。我们提出,这个层次化的转录网络构成了一个细胞周期调控机制,允许调节细胞大小和数量以实现稳健的器官生长。