Collaborative Research: Reducing complexity in vivo enables investigation of Cellulose Synthase-like D complex formation, trafficking and function

纤维素作为木材、纸张和纺织纤维的组成部分，具有重要的经济价值。它是在植物细胞壁中产生的，在那里它控制着生长和发育。制造大多数植物纤维素（CESAs）的酶以18组为一组产生葡萄糖链，并将它们捆绑在一起形成坚固耐用的微原纤维。相关酶（CSLDs）也产生葡萄糖链，但这些链是否捆绑在一起以及这如何影响最终产物的性质尚不清楚。csld是正常细胞分裂和某些形成长丝的植物细胞生长所必需的，这表明csld产生的纤维素的特殊性质对这些过程很重要。研究csld产生的纤维素的尝试受到CESAs产生的纤维素丰富的阻碍。虽然大多数植物没有CESAs就无法生存，但有可能产生缺乏CESAs的苔藓植物，从而仅依靠CSLDs获取纤维素。这些植物将用于研究csld及其生产的纤维素的结构和性质。植物细胞通过控制CESAs和CSLDs在时间和空间上的分布来调节其生长发育。细胞如何在正确的时间将这些酶传递到正确的位置，将通过在CESAs和CSLDs上添加荧光标记来研究。这项研究将有助于我们对植物生长的理解，以及我们如何改善商业植物纤维的性能。它还将通过培养本科生和研究生来建设科学人才队伍。该项目的目的是验证纤维素合酶样D （CSLD）蛋白形成纤维素合酶复合物并合成一种独特形式的微纤维纤维素的假设，并表征CSLD的功能分化和细胞靶向性，以阐明其在支持尖端生长和细胞分裂的特殊细胞壁结构域沉积中的作用。这项研究是通过敲除所有纤维素合成酶（CESA）基因的藓类Physcomitrium（以前的Physcomitrella）专利系进行的。这种独特的资源将用于研究体内CSLD的活性，而不受背景CESA活性的干扰。第一个目标是利用所有cesa基因敲除系通过冷冻断裂电子显微镜对含csld的膜复合物进行结构表征，并分离和分析csld产生的纤维素的结构。第二个目标是通过亚细胞蛋白定位和突变分析来表征CSLDs在原细胞尖端生长和细胞分裂中的作用。最终目的是利用强大的遗传和活细胞成像工具，确定靶向CSLDs和CESAs到质膜不同区域的细胞运输途径。通过定义CESAs和CSLDs之间的分工，本研究将加深对促进尖端生长和细胞分裂的特化细胞壁结构域的合成、结构和力学特性的理解，以及这些结构域如何促进整个生物体的形态发生。该奖项反映了美国国家科学基金会的法定使命，并通过使用基金会的知识价值和更广泛的影响审查标准进行评估，被认为值得支持。

Cellulose has important economic value as a component of wood, paper, and textile fibers. It is produced in the walls of plant cells, where it controls growth and development. The enzymes that make most plant cellulose (CESAs) produce chains of glucose in groups of 18 and bundle them together to form strong, durable microfibrils. Related enzymes (CSLDs) also produce chains of glucose, but whether these chains are bundled together and how this affects the properties of the final product is unknown. CSLDs are required for normal cell division and growth of certain plant cells that form long filaments, suggesting that special properties of the cellulose produced by CSLDs are important for these processes. Attempts to study the cellulose produced by CSLDs have been hampered by the abundance of cellulose produced by CESAs. Although most plants cannot survive without CESAs, it is possible to produce moss plants lacking CESAs thereby solely relying on CSLDs for cellulose. These plants will be used to study CSLDs and the structure and properties of the cellulose they produce. Plant cells regulate their growth and development by controlling the distribution of CESAs and CSLDs in time and space. How cells deliver these enzymes to the right place at the right time will be studied by adding fluorescent tags to CESAs and CSLDs. This research will contribute to our understanding of plant growth and how we might improve the properties of commercial plant fibers. It will also build the scientific workforce by training undergraduate and graduate students.The aims of this project are to test the hypothesis that Cellulose Synthase-like D (CSLD) proteins form cellulose synthase complexes and synthesize a distinct form of microfibrillar cellulose and to characterize the functional differentiation and cellular targeting of CSLDs to elucidate their roles in deposition of the specialized cell wall domains that support tip growth and cytokinesis. This research is enabled by lines of the moss Physcomitrium (formerly Physcomitrella) patens with all Cellulose Synthase (CESA) genes knocked out. This unique resource will be used to investigate CSLD activity in vivo without interference from background CESA activity. The first objective is to use the all cesa knockout lines to structurally characterize CSLD-containing membrane complexes by freeze fracture electron microscopy and to isolate and analyze the structure of the cellulose produced by CSLDs. The second objective is to characterize the roles of CSLDs in protonemal tip growth and cytokinesis by sub-cellular protein localization and mutation analysis. The final objective is to determine cellular trafficking pathways that target CSLDs and CESAs to distinct regions of the plasma membrane using the powerful genetic and live cell imaging tools possible in P. patens. By defining the division of labor between CESAs and CSLDs, this research will enhance understanding of the synthesis, structure and mechanical properties of the specialized cell wall domains that contribute to the regulation of tip growth and cytokinesis, and how these contribute to whole organism morphogenesis.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.