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本文引用的文献

1
The evaluation of pollen quality, and a further appraisal of the fluorochromatic (FCR) test procedure.花粉质量的评估,以及对荧光染色(FCR)测试程序的进一步评估。
Theor Appl Genet. 1984 Feb;67(4):367-75. doi: 10.1007/BF00272876.
2
Transcriptome analyses show changes in gene expression to accompany pollen germination and tube growth in Arabidopsis.转录组分析显示,拟南芥花粉萌发和花粉管生长过程中基因表达会发生变化。
Plant Physiol. 2008 Nov;148(3):1201-11. doi: 10.1104/pp.108.126375. Epub 2008 Sep 5.
3
The peroxin loss-of-function mutation abstinence by mutual consent disrupts male-female gametophyte recognition.过氧化物酶功能丧失突变导致的相互同意的禁欲会破坏雌雄配子体识别。
Curr Biol. 2008 Jan 8;18(1):63-8. doi: 10.1016/j.cub.2007.11.067. Epub 2007 Dec 20.
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Genetic subtraction profiling identifies genes essential for Arabidopsis reproduction and reveals interaction between the female gametophyte and the maternal sporophyte.遗传减法分析鉴定了拟南芥生殖所必需的基因,并揭示了雌配子体与母体孢子体之间的相互作用。
Genome Biol. 2007;8(10):R204. doi: 10.1186/gb-2007-8-10-r204.
5
Temperature as a determinant factor for increased and reproducible in vitro pollen germination in Arabidopsis thaliana.温度作为拟南芥体外花粉萌发增加且可重复的决定因素。
Plant J. 2007 Nov;52(3):570-82. doi: 10.1111/j.1365-313X.2007.03248.x. Epub 2007 Aug 30.
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The FERONIA receptor-like kinase mediates male-female interactions during pollen tube reception.FERONIA类受体激酶在花粉管接受过程中介导雌雄相互作用。
Science. 2007 Aug 3;317(5838):656-60. doi: 10.1126/science.1143562.
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Identification of genes expressed in the Arabidopsis female gametophyte.拟南芥雌配子体中表达基因的鉴定。
Plant J. 2007 Jul;51(2):281-92. doi: 10.1111/j.1365-313X.2007.03137.x. Epub 2007 Jun 8.
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9
RPA, a class II ARFGAP protein, activates ARF1 and U5 and plays a role in root hair development in Arabidopsis.RPA是一种II类ARFGAP蛋白,可激活ARF1和U5,并在拟南芥的根毛发育中发挥作用。
Plant Physiol. 2006 Jul;141(3):966-76. doi: 10.1104/pp.106.077818. Epub 2006 May 26.
10
Perturbation of rRNA synthesis in the bap28 mutation leads to apoptosis mediated by p53 in the zebrafish central nervous system.bap28突变中rRNA合成的扰动导致斑马鱼中枢神经系统中由p53介导的细胞凋亡。
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与拟南芥雄配子体发育和功能缺陷相关的Ds插入突变体集合。

A collection of Ds insertional mutants associated with defects in male gametophyte development and function in Arabidopsis thaliana.

作者信息

Boavida Leonor C, Shuai Bin, Yu Hee-Ju, Pagnussat Gabriela C, Sundaresan Venkatesan, McCormick Sheila

机构信息

Plant Gene Expression Center and Plant and Microbial Biology, US Department of Agriculture/Agricultural Research Service, Albany, California 94710, USA.

出版信息

Genetics. 2009 Apr;181(4):1369-85. doi: 10.1534/genetics.108.090852. Epub 2009 Feb 23.

DOI:10.1534/genetics.108.090852
PMID:19237690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2666506/
Abstract

Functional analyses of the Arabidopsis genome require analysis of the gametophytic generation, since approximately 10% of the genes are expressed in the male gametophyte and approximately 9% in the female gametophyte. Here we describe the genetic and molecular characterization of 67 Ds insertion lines that show reduced transmission through the male gametophyte. About half of these mutations are male gametophytic-specific mutations, while the others also affect female transmission. Genomic sequences flanking both sides of the Ds element were recovered for 39 lines; for 16 the Ds elements were inserted in or close to coding regions, while 7 were located in intergenic/unannotated regions of the genome. For the remaining 16 lines, chromosomal rearrangements such as translocations or deletions, ranging between 30 and 500 kb, were associated with the transposition event. The mutants were classified into five groups according to the developmental processes affected; these ranged from defects in early stages of gametogenesis to later defects affecting pollen germination, pollen tube growth, polarity or guidance, or pollen tube-embryo sac interactions or fertilization. The isolated mutants carry Ds insertions in genes with diverse biological functions and potentially specify new functions for several unannotated or unknown proteins.

摘要

对拟南芥基因组进行功能分析需要对配子体世代进行分析,因为约10%的基因在雄配子体中表达,约9%在雌配子体中表达。本文我们描述了67个Ds插入系的遗传和分子特征,这些插入系通过雄配子体的传递率降低。这些突变中约一半是雄配子体特异性突变,而其他突变也影响雌配子体的传递。对39个品系回收了Ds元件两侧的基因组序列;其中16个品系的Ds元件插入到编码区或其附近,7个位于基因组的基因间/未注释区域。对于其余16个品系,30至500 kb范围内的染色体重排如易位或缺失与转座事件相关。根据受影响的发育过程,将这些突变体分为五组;这些过程从配子发生早期的缺陷到影响花粉萌发、花粉管生长、极性或导向,或花粉管-胚囊相互作用或受精的后期缺陷不等。分离得到的突变体在具有不同生物学功能的基因中携带Ds插入,并且可能为几种未注释或未知的蛋白质确定新功能。