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果蝇卵母细胞中无义mRNA的定位。

Gratuitous mRNA localization in the Drosophila oocyte.

作者信息

Serano T L, Cohen R S

机构信息

Department of Biochemistry, University of Kansas, Lawrence 66045, USA.

出版信息

Development. 1995 Sep;121(9):3013-21. doi: 10.1242/dev.121.9.3013.

DOI:10.1242/dev.121.9.3013
PMID:7555727
Abstract

Many of the genes that control pattern formation in Drosophila encode mRNAs that are localized to discrete regions of the oocyte during oogenesis. While such localization is generally assumed to be important for the pattern-forming activities of these genes, this has been rigorously demonstrated in only a few cases. Here we address the role of mRNA localization for the dorsoventral patterning gene K10. K10 mRNA is localized to the oocyte's anterior cortex following its transport into the cell during early stages of oogenesis. We show that mutations in cappuccino and spire, which permit K10 mRNA transport, but prevent subsequent anterior localization, do not disrupt the synthesis or localization of K10 protein. We also show that modified K10 transgenes that produce transcripts which are uniformly distributed throughout the oocyte, or which are mislocalized to the oocyte's posterior pole, produce localized and functional K10 protein. We conclude that the anterior localization of K10 mRNA is not important for K10 protein targeting or gene function. We propose that the anterior localization of K10, and probably other mRNAs, is a by-product of mRNA transport and does not necessarily reflect a requirement for localization per se.

摘要

许多控制果蝇模式形成的基因编码的mRNA在卵子发生过程中定位于卵母细胞的离散区域。虽然一般认为这种定位对于这些基因的模式形成活动很重要,但仅在少数情况下得到了严格证明。在这里,我们探讨mRNA定位对背腹模式形成基因K10的作用。K10 mRNA在卵子发生早期被转运到细胞中后定位于卵母细胞的前皮质。我们表明,卡布奇诺和螺旋蛋白中的突变允许K10 mRNA转运,但阻止随后的前侧定位,不会破坏K10蛋白的合成或定位。我们还表明,产生的转录本在整个卵母细胞中均匀分布或错误定位于卵母细胞后极的修饰K10转基因产生定位且有功能的K10蛋白。我们得出结论,K10 mRNA的前侧定位对于K10蛋白靶向或基因功能并不重要。我们提出,K10以及可能其他mRNA的前侧定位是mRNA转运的副产物,不一定反映对定位本身的需求。

相似文献

1
Gratuitous mRNA localization in the Drosophila oocyte.果蝇卵母细胞中无义mRNA的定位。
Development. 1995 Sep;121(9):3013-21. doi: 10.1242/dev.121.9.3013.
2
A small predicted stem-loop structure mediates oocyte localization of Drosophila K10 mRNA.一个小的预测茎环结构介导果蝇K10 mRNA的卵母细胞定位。
Development. 1995 Nov;121(11):3809-18. doi: 10.1242/dev.121.11.3809.
3
Comparative analysis of the kinetics and dynamics of K10, bicoid, and oskar mRNA localization in the Drosophila oocyte.果蝇卵母细胞中K10、双尾和 Oskar mRNA 定位的动力学和动态学的比较分析。
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7
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引用本文的文献

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In vivo imaging of oskar mRNA transport reveals the mechanism of posterior localization.对osk基因信使核糖核酸转运的体内成像揭示了其在细胞后部定位的机制。
Cell. 2008 Sep 5;134(5):843-53. doi: 10.1016/j.cell.2008.06.053.
2
The positional, structural, and sequence requirements of the Drosophila TLS RNA localization element.果蝇TLS RNA定位元件的位置、结构和序列要求。
RNA. 2005 Jul;11(7):1017-29. doi: 10.1261/rna.7218905.
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Recognition of the bcd mRNA localization signal in Drosophila embryos and ovaries.果蝇胚胎和卵巢中bcd mRNA定位信号的识别。
Mol Cell Biol. 2005 Feb;25(4):1501-10. doi: 10.1128/MCB.25.4.1501-1510.2005.
4
The Drosophila synaptotagmin-like protein bitesize is required for growth and has mRNA localization sequences within its open reading frame.果蝇中与突触结合蛋白相似的蛋白“bitesize”对生长是必需的,并且在其开放阅读框内具有mRNA定位序列。
Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13368-73. doi: 10.1073/pnas.1835727100. Epub 2003 Oct 27.
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Widespread cytoplasmic mRNA transport in yeast: identification of 22 bud-localized transcripts using DNA microarray analysis.酵母中广泛存在的细胞质mRNA转运:利用DNA微阵列分析鉴定22个芽定位转录本
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6
Localization-dependent translation requires a functional interaction between the 5' and 3' ends of oskar mRNA.依赖定位的翻译需要oskar mRNA的5'端和3'端之间进行功能性相互作用。
Genes Dev. 1998 Jun 1;12(11):1652-64. doi: 10.1101/gad.12.11.1652.