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本文引用的文献

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The Cauliflower Mosaic Virus 35S Promoter: Combinatorial Regulation of Transcription in Plants.花椰菜花叶病毒35S启动子:植物转录的组合调控
Science. 1990 Nov 16;250(4983):959-66. doi: 10.1126/science.250.4983.959.
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Small cysteine-rich peptides resembling antimicrobial peptides have been under-predicted in plants.在植物中,类似于抗菌肽的富含半胱氨酸的小肽一直未得到充分预测。
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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。
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Interaction between rice MYBGA and the gibberellin response element controls tissue-specific sugar sensitivity of alpha-amylase genes.水稻MYBGA与赤霉素反应元件之间的相互作用控制α-淀粉酶基因的组织特异性糖敏感性。
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EST generation and analyses towards identifying female gametophyte-specific genes in Zea mays L.为鉴定玉米中的雌配子体特异性基因而进行的EST生成与分析
Planta. 2006 Oct;224(5):1004-14. doi: 10.1007/s00425-006-0283-3. Epub 2006 May 23.
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trans meets cis in MADS science.在MADS科学领域中,跨性别者与顺性别者相遇。
Trends Plant Sci. 2006 May;11(5):224-31. doi: 10.1016/j.tplants.2006.03.008. Epub 2006 Apr 17.
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Cell-cell communication during double fertilization.双受精过程中的细胞间通讯。
Curr Opin Plant Biol. 2006 Feb;9(1):41-7. doi: 10.1016/j.pbi.2005.11.002. Epub 2005 Dec 1.
8
MYB98 is required for pollen tube guidance and synergid cell differentiation in Arabidopsis.拟南芥中的花粉管导向和助细胞分化需要MYB98。
Plant Cell. 2005 Nov;17(11):2981-92. doi: 10.1105/tpc.105.034603. Epub 2005 Oct 7.
9
The WEREWOLF MYB protein directly regulates CAPRICE transcription during cell fate specification in the Arabidopsis root epidermis.在拟南芥根表皮细胞命运特化过程中,狼人MYB蛋白直接调控CAPRICE转录。
Development. 2005 Nov;132(21):4765-75. doi: 10.1242/dev.02055. Epub 2005 Oct 5.
10
Construction and screening of subtracted cDNA libraries from limited populations of plant cells: a comparative analysis of gene expression between maize egg cells and central cells.从有限数量的植物细胞构建和筛选消减cDNA文库:玉米卵细胞与中央细胞之间基因表达的比较分析
Plant J. 2005 Oct;44(1):167-78. doi: 10.1111/j.1365-313X.2005.02518.x.

MYB98正向调控一系列由助细胞表达的、编码丝状器定位蛋白的基因。

MYB98 positively regulates a battery of synergid-expressed genes encoding filiform apparatus localized proteins.

作者信息

Punwani Jayson A, Rabiger David S, Drews Gary N

机构信息

Department of Biology, University of Utah, Salt Lake City, Utah 84112-0840, USA.

出版信息

Plant Cell. 2007 Aug;19(8):2557-68. doi: 10.1105/tpc.107.052076. Epub 2007 Aug 10.

DOI:10.1105/tpc.107.052076
PMID:17693534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2002610/
Abstract

The synergid cells within the female gametophyte are essential for reproduction in angiosperms. MYB98 encodes an R2R3-MYB protein required for pollen tube guidance and filiform apparatus formation by the synergid cells. To test the predicted function of MYB98 as a transcriptional regulator, we determined its subcellular localization and examined its DNA binding properties. We show that MYB98 binds to a specific DNA sequence (TAAC) and that a MYB98-green fluorescent protein fusion protein localizes to the nucleus, consistent with a role in transcriptional regulation. To identify genes regulated by MYB98, we tested previously identified synergid-expressed genes for reduced expression in myb98 female gametophytes and identified 16 such genes. We dissected the promoter of one of the downstream genes, DD11, and show that it contains a MYB98 binding site required for synergid expression, suggesting that DD11 is regulated directly by MYB98. To gain insight into the functions of the downstream genes, we chose five genes and determined the subcellular localization of the encoded proteins. We show that these five proteins are secreted into the filiform apparatus, suggesting that they play a role in either the formation or the function of this unique structure. Together, these data suggest that MYB98 functions as a transcriptional regulator in the synergid cells and activates the expression of genes required for pollen tube guidance and filiform apparatus formation.

摘要

雌配子体中的助细胞对于被子植物的繁殖至关重要。MYB98编码一种R2R3-MYB蛋白,该蛋白是助细胞引导花粉管生长和形成丝状器所必需的。为了验证MYB98作为转录调节因子的预测功能,我们确定了其亚细胞定位并检测了其DNA结合特性。我们发现MYB98能结合特定的DNA序列(TAAC),并且MYB98-绿色荧光蛋白融合蛋白定位于细胞核,这与它在转录调节中的作用一致。为了鉴定受MYB98调控的基因,我们检测了先前鉴定的在助细胞中表达的基因在myb98雌配子体中的表达是否降低,并鉴定出16个这样的基因。我们剖析了其中一个下游基因DD11的启动子,发现它含有助细胞表达所需的MYB98结合位点,这表明DD11直接受MYB98调控。为了深入了解下游基因的功能,我们选择了五个基因并确定了它们编码蛋白的亚细胞定位。我们发现这五种蛋白都分泌到丝状器中,这表明它们在这个独特结构的形成或功能中发挥作用。总之,这些数据表明MYB98在助细胞中作为转录调节因子发挥作用,并激活花粉管引导和丝状器形成所需基因的表达。