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国家重点基础研究发展计划(2011CB100203)

作品数:4 被引量:159H指数:4
相关作者:王慧娜马兴亮初志战李日清刘耀光更多>>
相关机构:华南农业大学更多>>
发文基金:国家重点基础研究发展计划更多>>
相关领域:农业科学生物学更多>>

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Molecular Control of Male Reproductive Development and Pollen Fertility in Rice被引量:20
2012年
Anther development and male fertility are essential biological pro- cesses for flowering plants and are important for crop seed produc- tion. Genetic manipulation of male fertility/sterility is critical for crop hybrid breeding. Rice (Oryza sativa L.) male sterility phenotypes, including genic male sterility, hybrid male sterility, and cytoplasmic male sterility, are generally caused by mutations of fertility-related genes, by incompatible interactions between divergent allelic or non-allelic genes, or by genetic incompatibilities between cytoplas-mic and nuclear genomes. Here, we review the recent advances in the molecular basis of anther development and male fertility-sterility conversion in specific genetic backgrounds, and the interactions with certain environmental factors. The highlighted findings in this review have significant implications in both basic studies and rice genetic improvement.
Jing-Xin GuoYao-Guang Liu
关键词:MEIOSIS
A Novel Rice bHLH Transcription Factor, DTD, Acts Coordinately with TDR in Controlling Tapetum Function and Pollen Development被引量:20
2013年
Dear Editor, Male reproductive development is an essential biological process for flowering plants and crucial for crop seed produc- tion. Formation of the male reproductive organ, the anther, involves a number of developmental events, including sta- men meristem specification, generation of sporogenous cells and their differentiation into microspore mother cells (MMCs), meiosis, microspore (pollen) maturation, and polli- nation (Ma, 2005). The formation of microspores and their development into mature pollen grains require cooperative interactions between gametophytic (microspores) and sporo- phytic (anther wall) cells, with the innermost cell layer, the tapetum, playing the most crucial role (Ma, 2005). Tapetal cells underao decleneration bv Droclrammed cell death (PCD).
Chonghui Ji Heying Li Libin Chen Min Xie Fengping Wang Yuanling Chen Yao-Guang Liu
高通量PCR模板植物基因组DNA制备方法被引量:19
2013年
制备大量生物样品的模板DNA用于PCR检测是费时费工的工作。本文介绍一种快速高通量的植物基因组DNA(gDNA)制备及其用于PCR基因型检测的操作方法。将一小段单子叶植物苗叶片(与96方孔板的孔深大致相同)或一小块(约2~5mg)双子叶植物叶片放入96方孔板的各孔中、放入一粒直径4mm或3mm的合金珠和150μL制备缓冲液,盖上硅橡胶盖,在涡旋器或震动研磨器震动2~4min破碎组织。此方法获得的粗制gDNA样品浓度约2~4ngμL?1。用96针复制器或多通道移液器转移约0.5~1.0μL的gDNA溶液到96孔PCR板的反应液中,利用各种类型的PCR标记(简单序列重复SSR,插入缺失InDel等)进行基因型检测。此方法制备的gDNA模板也适合于较大DNA片段(>1kb)的扩增。本方法的关键是控制好在一定溶液量中破碎合适量的叶片,以及不要加入过量的gDNA溶液,以免带入过多的杂质抑制PCR效果。这种从材料种植、制备gDNA、转移样品gDNA,到PCR都是96格式化操作的快速、高通量、低成本的方法特别适合大量植物样品的规模化基因型检测。
王慧娜初志战马兴亮李日清刘耀光
关键词:PCR基因分型
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