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红花(Carthamus tinctorius L.)的花药、花粉和绒毡层发育

Anther, pollen and tapetum development in safflower, Carthamus tinctorius L.

作者信息

Yeung Edward C, Oinam Gunamani S, Yeung Stephanie S, Harry Indra

机构信息

Department of Biological Sciences, University of Calgary, Calgary, AB T2N 1N4, Canada.

出版信息

Sex Plant Reprod. 2011 Dec;24(4):307-17. doi: 10.1007/s00497-011-0168-x. Epub 2011 May 15.

Abstract

In safflower, the anther wall at maturity consists of a single epidermis, an endothecium, a middle layer and the tapetum. The tapetum consists mainly of a single layer of cells. However, this single-layer appearance is punctuated by loci having 'two-celled' groupings due to additional periclinal divisions in some tapetal cells. Meiotic division in microsporocytes gives rise to tetrads of microspores. The primexine is formed around the protoplasts of microspores while they are still enveloped within the callose wall. Just prior to microgametogenesis, the microspores enlarge through the process of vacuolation, and the exine wall pattern becomes established. Microgametogenesis results in the formation of 3-celled pollen grains. The two elongated sperm cells appear to be connected. The exine wall is highly sculptured with a distinct tectum, columellae, a foot layer, an endexine and a thin intine. Similar to other members of the Asteraceae family, the tapetum is of the invasive type. The most novel finding of this study is that in addition to the presence of invasive tapetal cells, a small population of 'non-invasive' tapetal cells is also present. The tapetal cells next to the anther locules in direct contact with the microspores become invasive and start to grow into the space between developing microspores. These tapetal cells synthesize tryphine and eventually degenerate at the time of gametogenesis releasing their content into the anther locules. A smaller population of non-invasive tapetal cells is formed as a result of periclinal divisions at the time of tapetum differentiation. These cells are not exposed to the anther locules until the degeneration of the invasive tapetal cells. The non-invasive tapetal cells have a different cell fate as they synthesize pollenkitt. This material is responsible for allowing some pollen grains to adhere to each other and to the anther wall after anther dehiscence. This observation explains the out-crossing ability of Carthamus species and varieties in nature.

摘要

在红花中,成熟花药壁由单层表皮、药室内壁、中层和绒毡层组成。绒毡层主要由单层细胞构成。然而,由于部分绒毡层细胞发生额外的平周分裂,这种单层外观会被具有“双细胞”组合的位点打断。小孢子母细胞的减数分裂产生四分体小孢子。当小孢子原生质体仍被胼胝质壁包裹时,初生外壁在其周围形成。就在小孢子发生之前,小孢子通过液泡化过程增大,外壁图案形成。小孢子发生导致形成三细胞花粉粒。两个细长的精细胞似乎相连。外壁高度纹饰化,具有明显的覆盖层、柱状层、基足层、内壁层和薄的内壁。与菊科其他成员类似,绒毡层为侵入型。本研究最新颖的发现是,除了存在侵入性绒毡层细胞外,还存在一小部分“非侵入性”绒毡层细胞。与小孢子直接接触的花药室旁的绒毡层细胞变为侵入性,并开始生长到发育中的小孢子之间的空间。这些绒毡层细胞合成类胡萝卜素,最终在配子发生时退化,将其内含物释放到花药室中。一小部分非侵入性绒毡层细胞是绒毡层分化时平周分裂的结果。这些细胞在侵入性绒毡层细胞退化之前不会暴露于花药室。非侵入性绒毡层细胞具有不同的细胞命运,因为它们合成花粉块柄物质。这种物质使得一些花粉粒在花药开裂后能够相互粘附并粘附在花药壁上。这一观察结果解释了红花属物种和变种在自然环境中的异交能力。

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