胼胝质
胞间连丝
生物
韧皮部
细胞生物学
内胚层
形态发生
植物
拟南芥
基因
细胞质
生物化学
细胞壁
突变体
作者
Anne Vatén,Jan Dettmer,Shuang Wu,York‐Dieter Stierhof,Shunsuke Miyashima,Shri Ram Yadav,Christina Roberts,Ana Campilho,Vincent Bulone,Raffael Lichtenberger,Satu Lehesranta,Ari Pekka Mähönen,Jae‐Yean Kim,Eija Jokitalo,Norbert Sauer,Ben Scheres,Keiji Nakajima,Annelie Carlsbecker,Kimberly L. Gallagher,Ykä Helariutta
标识
DOI:10.1016/j.devcel.2011.10.006
摘要
Plant cells are connected through plasmodesmata (PD), membrane-lined channels that allow symplastic movement of molecules between cells. However, little is known about the role of PD-mediated signaling during plant morphogenesis. Here, we describe an Arabidopsis gene, CALS3/GSL12. Gain-of-function mutations in CALS3 result in increased accumulation of callose (β-1,3-glucan) at the PD, a decrease in PD aperture, defects in root development, and reduced intercellular trafficking. Enhancement of CALS3 expression during phloem development suppressed loss-of-function mutations in the phloem abundant callose synthase, CALS7 indicating that CALS3 is a bona fide callose synthase. CALS3 alleles allowed us to spatially and temporally control the PD aperture between plant tissues. Using this tool, we are able to show that movement of the transcription factor SHORT-ROOT and microRNA165 between the stele and the endodermis is PD dependent. Taken together, we conclude that regulated callose biosynthesis at PD is essential for cell signaling.
科研通智能强力驱动
Strongly Powered by AbleSci AI