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本文引用的文献

1
fs(1)K10, a germline-dependent female sterile mutation causing abnormal chorion morphology inDrosophila melanogaster.fs(1)K10,一种依赖种系的雌性不育突变,可导致黑腹果蝇的绒毛膜形态异常。
Wilehm Roux Arch Dev Biol. 1978 Mar;184(1):75-82. doi: 10.1007/BF00848670.
2
A repeated IMP-binding motif controls oskar mRNA translation and anchoring independently of Drosophila melanogaster IMP.一个重复的IMP结合基序独立于黑腹果蝇IMP控制oskar mRNA的翻译和锚定。
J Cell Biol. 2006 Feb 13;172(4):577-88. doi: 10.1083/jcb.200510044.
3
The RNA-binding protein Squid is required for the establishment of anteroposterior polarity in the Drosophila oocyte.RNA结合蛋白鱿鱼对于果蝇卵母细胞前后极性的建立是必需的。
Development. 2005 Dec;132(24):5515-25. doi: 10.1242/dev.02159. Epub 2005 Nov 16.
4
gurken and the I factor retrotransposon RNAs share common localization signals and machinery.gurken与I因子逆转录转座子RNA共享共同的定位信号和机制。
Dev Cell. 2005 Jul;9(1):51-62. doi: 10.1016/j.devcel.2005.04.012.
5
Squid is required for efficient posterior localization of oskar mRNA during Drosophila oogenesis.在果蝇卵子发生过程中,鱿鱼蛋白对于osk基因mRNA高效地定位到卵子后端是必需的。
Dev Genes Evol. 2005 Jul;215(7):340-9. doi: 10.1007/s00427-005-0480-2. Epub 2005 Mar 25.
6
Genetic interactions of Drosophila melanogaster arrest reveal roles for translational repressor Bruno in accumulation of Gurken and activity of Delta.黑腹果蝇发育停滞的基因相互作用揭示了翻译抑制因子布鲁诺在 Gurken 积累和 Delta 活性中的作用。
Genetics. 2004 Nov;168(3):1433-42. doi: 10.1534/genetics.104.033985.
7
Hrp48, a Drosophila hnRNPA/B homolog, binds and regulates translation of oskar mRNA.Hrp48是一种果蝇hnRNPA/B同源物,它结合并调节oskar mRNA的翻译。
Dev Cell. 2004 May;6(5):637-48. doi: 10.1016/s1534-5807(04)00132-7.
8
The Drosophila hnRNPA/B homolog, Hrp48, is specifically required for a distinct step in osk mRNA localization.果蝇的hnRNPA/B同源物Hrp48,是osk mRNA定位过程中一个特定步骤所特别需要的。
Dev Cell. 2004 May;6(5):625-35. doi: 10.1016/s1534-5807(04)00130-3.
9
Live imaging of nuage and polar granules: evidence against a precursor-product relationship and a novel role for Oskar in stabilization of polar granule components.生殖质和极颗粒的实时成像:反对前体-产物关系的证据以及Oskar在稳定极颗粒成分中的新作用。
J Cell Sci. 2004 Apr 15;117(Pt 10):2109-20. doi: 10.1242/jcs.01059.
10
Hrb27C, Sqd and Otu cooperatively regulate gurken RNA localization and mediate nurse cell chromosome dispersion in Drosophila oogenesis.Hrb27C、Sqd和Otu协同调节果蝇卵子发生过程中gurken RNA的定位,并介导滋养细胞染色体分散。
Development. 2004 May;131(9):1949-58. doi: 10.1242/dev.01078. Epub 2004 Mar 31.

Imp与鱿鱼和Hrp48相关联,并有助于gurken在卵母细胞中的局部表达。

Imp associates with squid and Hrp48 and contributes to localized expression of gurken in the oocyte.

作者信息

Geng Cuiyun, Macdonald Paul M

机构信息

Institute for Cellular and Molecular Biology, Section of Molecular Cell and Developmental Biology, The University of Texas at Austin, Austin, TX 78712-0159, USA.

出版信息

Mol Cell Biol. 2006 Dec;26(24):9508-16. doi: 10.1128/MCB.01136-06. Epub 2006 Oct 9.

DOI:10.1128/MCB.01136-06
PMID:17030623
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1698525/
Abstract

Localization and translational control of Drosophila melanogaster gurken and oskar mRNAs rely on the hnRNP proteins Squid and Hrp48, which are complexed with one another in the ovary. Imp, the Drosophila homolog of proteins acting in localization of mRNAs in other species, is also associated with Squid and Hrp48. Notably, Imp is concentrated at sites of gurken and oskar mRNA localization in the oocyte, and alteration of gurken localization also alters Imp distribution. Imp binds gurken mRNA with high affinity in vitro; thus, the colocalization with gurken mRNA in vivo is likely to be the result of direct binding. Imp mutants support apparently normal regulation of gurken and oskar mRNAs. However, loss of Imp activity partially suppresses a gurken misexpression phenotype, indicating that Imp does act in control of gurken expression but has a largely redundant role that is only revealed when normal gurken expression is perturbed. Overexpression of Imp disrupts localization of gurken mRNA as well as localization and translational regulation of oskar mRNA. The opposing effects of reduced and elevated Imp activity on gurken mRNA expression indicate a role in gurken mRNA regulation.

摘要

黑腹果蝇中gurken和oskar mRNA的定位及翻译控制依赖于hnRNP蛋白Squid和Hrp48,它们在卵巢中相互结合。Imp是其他物种中参与mRNA定位的蛋白质的果蝇同源物,也与Squid和Hrp48相关联。值得注意的是,Imp集中在卵母细胞中gurken和oskar mRNA的定位位点,gurken定位的改变也会改变Imp的分布。Imp在体外以高亲和力结合gurken mRNA;因此,在体内与gurken mRNA的共定位可能是直接结合的结果。Imp突变体表面上支持gurken和oskar mRNA的正常调控。然而,Imp活性的丧失部分抑制了gurken错误表达表型,表明Imp确实在控制gurken表达中起作用,但具有很大程度上的冗余作用,只有在正常的gurken表达受到干扰时才会显现出来。Imp的过表达会破坏gurken mRNA的定位以及oskar mRNA的定位和翻译调控。Imp活性降低和升高对gurken mRNA表达的相反作用表明其在gurken mRNA调控中发挥作用。