Wightman Raymond, Marshall Robin, Turner Simon R
Faculty of Life Sciences, University of Manchester, Manchester M139PT, UK.
Plant Cell Physiol. 2009 Mar;50(3):584-94. doi: 10.1093/pcp/pcp017. Epub 2009 Feb 2.
The woody secondary walls of plants represent the major sites of cellulose deposition. The polymerization of cellulose occurs at the plasma membrane by the secondary wall cellulose synthase complex (CSC). In the long, cylindrical cells that make up the xylem, secondary wall deposition is confined to discrete regions of the cell, and yellow fluorescent protein (YFP)-labeled CSCs are also localized to these regions. Using fluorescence loss in photobleaching (FLIP) of complete hoops containing YFP-CSCs, we demonstrate movement of the complexes beneath the nascent secondary wall in developing xylem vessels. We have devised a method for determining particle velocities for particles moving around a cylindrical object using data from FLIP. By applying this method to the hoops of YFP-CSCs of the developing vessels, we have obtained the first estimates of speed of these complexes. These speeds are calculated to be in excess of 7 microm s(-1) and are far higher than those speeds previously reported for the primary wall complex. These high speeds are unlikely to be consistent with CSC movement being attributed to cellulose synthesis alone, and suggest the existence of a highly motile compartment beneath the nascent secondary wall.
植物的木质次生壁是纤维素沉积的主要部位。纤维素的聚合在质膜上由次生壁纤维素合酶复合体(CSC)完成。在构成木质部的长圆柱形细胞中,次生壁沉积局限于细胞的离散区域,黄色荧光蛋白(YFP)标记的CSC也定位于这些区域。通过对含有YFP-CSC的完整环进行光漂白荧光损失(FLIP)实验,我们证明了在发育中的木质部导管中,复合体在新生次生壁下方移动。我们设计了一种方法,利用FLIP数据确定围绕圆柱形物体移动的粒子速度。通过将该方法应用于发育中导管的YFP-CSC环,我们首次估算了这些复合体的速度。计算得出这些速度超过7微米每秒(-1),远高于先前报道的初生壁复合体速度。这些高速不太可能与仅归因于纤维素合成的CSC移动相一致,这表明在新生次生壁下方存在一个高度活跃的区域。