INRAE, UMR1332 Biologie du Fruit et Pathologie, Université Bordeaux, Villenave d'Ornon F-33140, France.
CNRS, UMR5200 Laboratoire de Biogenèse Membranaire, Université Bordeaux, Villenave d'Ornon F-33140, France.
Plant Physiol. 2024 Oct 1;196(2):883-901. doi: 10.1093/plphys/kiae198.
FW2.2 (standing for FRUIT WEIGHT 2.2), the founding member of the CELL NUMBER REGULATOR (CNR) gene family, was the first cloned gene underlying a quantitative trait locus (QTL) governing fruit size and weight in tomato (Solanum lycopersicum). However, despite this discovery over 20 yr ago, the molecular mechanisms by which FW2.2 negatively regulates cell division during fruit growth remain undeciphered. In the present study, we confirmed that FW2.2 is a membrane-anchored protein whose N- and C-terminal ends face the apoplast. We unexpectedly found that FW2.2 is located at plasmodesmata (PD). FW2.2 participates in the spatiotemporal regulation of callose deposition at PD and belongs to a protein complex which encompasses callose synthases. These results suggest that FW2.2 has a regulatory role in cell-to-cell communication by modulating PD transport capacity and trafficking of signaling molecules during fruit development.
FW2.2(代表果实重量 2.2)是细胞数量调节因子(CNR)基因家族的创始成员,它是第一个克隆的基因,该基因位于控制番茄(Solanum lycopersicum)果实大小和重量的数量性状位点(QTL)之下。然而,尽管这一发现已经过去了 20 多年,但 FW2.2 如何负调控果实生长过程中的细胞分裂的分子机制仍未被破译。在本研究中,我们证实 FW2.2 是一种膜锚定蛋白,其 N 端和 C 端朝向质外体。我们意外地发现 FW2.2 位于胞间连丝(PD)上。FW2.2 参与 PD 处胼胝质沉积的时空调节,属于包含胼胝质合酶的蛋白质复合物。这些结果表明,FW2.2 通过调节 PD 运输能力和信号分子在果实发育过程中的运输,在细胞间通讯中发挥调节作用。