Growth and development of conifer pollen tubes

被引:85
作者
Fernando D.D. [1 ]
Lazzaro M.D. [2 ]
Owens J.N. [3 ]
机构
[1] Department of Environmental and Forest Biology, State University of New York, College of Environmental Science and Forestry, Syracuse, NY 13210
[2] Department of Biology, College of Charleston, Charleston, SC 29424
[3] Centre for Forest Biology, University of Victoria, Victoria
来源
Sexual Plant Reproduction | 2005年 / 18卷 / 4期
关键词
Conifers; Gymnosperm reproduction; Microgametogenesis; Microsporogenesis; Pollen; Pollen tubes;
D O I
10.1007/s00497-005-0008-y
中图分类号
学科分类号
摘要
Conifer pollen tubes are an important but underused experimental system in plant biology. They represent a major evolutionary step in male gametophyte development as an intermediate form between the haustorial pollen tubes of cycads and Ginkgo and the structurally reduced and faster growing pollen tubes of flowering plants. Conifer pollen grains are available in large quantities, most can be stored for several years, and they grow very well in culture. The study of pollen tube growth and development furthers our understanding of conifer reproduction and contributes towards our ability to improve on their productivity. This review covers taxonomy and morphology to cell, developmental, and molecular biology. It explores recent advances in research on conifer pollen and pollen tubes in vivo, focusing on pollen wall structure, male gametophyte development within the pollen wall, pollination mechanisms, pollen tube growth and development, and programmed cell death. It also explores recent research in vitro, including the cellular mechanisms underlying pollen tube elongation, in vitro fertilization, genetic transformation and gene expression, and pine pollen tube proteomics. With the ongoing sequencing of the Pinus taeda genome in several labs, we expect the use of conifer pollen tubes as an experimental system to increase in the next decade. © Springer-Verlag 2005.
引用
收藏
页码:149 / 162
页数:13
相关论文
共 84 条
[1]  
Anderhag P., Hepler P.K., Lazzaro M.D., Microtubules and microfilaments are both responsible for pollen tube elongation in the conifer Picea abies (Norway spruce), Protoplasma, 214, pp. 141-157, (2000)
[2]  
Anderson E.D., Owens J.N., Microsporogenesis, pollination, pollen germination and male gametophyte development in Taxus brevifolia, Ann Bot, 86, pp. 1033-1044, (2000)
[3]  
Anderson E.D., Owens J.N., Colangeli A.M., Russell J.H., Challenges facing yellow cypress (Chamaecyparis nootkatensis) seed orchards: Low filled seed production, pollen-cone abortion, self-pollination, and accelerated embryo development, Can J For Res, 32, pp. 1411-1419, (2002)
[4]  
Aronen T.S., Nikkanen T.O., Haggman H.M., Compatibility of different pollination techniques with microprojectile bombardment of Norway spruce and Scots pine pollen, Can J For Res, 28, pp. 79-86, (1998)
[5]  
Aronen T.S., Nikkanen T.O., Haggman H.M., The production of transgenic Scots pine (Pinus sylvestris L.) via the application of transformed pollen in controlled crossings, Trans Res, 12, pp. 375-378, (2003)
[6]  
Bahrman N., Petit R.J., Genetic polymorphism in maritime pine (Pinus pinaster Ait.) assessed by two-dimensional gel electrophoresis of needle, bud and pollen proteins, J Mol Evol, 41, pp. 231-237, (1995)
[7]  
Bruns D., Owens J.N., Western white pine (Pinus monticola) reproduction: II. Fertilization and cytoplasmic inheritance, Sex Plant Reprod, 13, pp. 75-84, (2000)
[8]  
Carpita N.C., Gibeaut D.M., Structural models of primary cell walls in flowering plants: Consistency of molecular structure with the physical properties of the walls during growth, Plant J, 3, pp. 1-30, (1993)
[9]  
Chandler L.M., Owens J.N., The pollination mechanism in Abies amabilis, Can J For Res, 34, pp. 1-10, (2004)
[10]  
Colangeli A.M., Owens J.N., Post-dormancy seed-cone development and the pollination mechanism in western hemlock (Tsuga heterophylla), Can J For Res, 19, pp. 44-53, (1989)