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Rescue of a dominant mutant with RNA interference.用 RNA 干扰拯救显性突变体。
Genetics. 2010 Dec;186(4):1493-6. doi: 10.1534/genetics.110.123471. Epub 2010 Sep 27.
2
A new opaque variant of maize by a single dominant RNA-interference-inducing transgene.一种由单个显性RNA干扰诱导转基因产生的新型不透明玉米变种。
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Synthesis of an unusual alpha-zein protein is correlated with the phenotypic effects of the floury2 mutation in maize.一种不寻常的α-玉米醇溶蛋白的合成与玉米粉质2突变的表型效应相关。
Mol Gen Genet. 1994 Dec 1;245(5):537-47. doi: 10.1007/BF00282216.
4
Expression of a mutant alpha-zein creates the floury2 phenotype in transgenic maize.突变α-醇溶蛋白的表达在转基因玉米中产生粉质2表型。
Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):7094-7. doi: 10.1073/pnas.94.13.7094.
5
RNA interference-mediated change in protein body morphology and seed opacity through loss of different zein proteins.通过不同的醇溶蛋白缺失导致的蛋白体形态和种子不透明性的 RNA 干扰介导的变化。
Plant Physiol. 2010 May;153(1):337-47. doi: 10.1104/pp.110.154690. Epub 2010 Mar 17.
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Balancing of sulfur storage in maize seed.平衡玉米种子中的硫储存。
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NAC-type transcription factors regulate accumulation of starch and protein in maize seeds.NAC 型转录因子调节玉米种子中淀粉和蛋白质的积累。
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Compositional and transcriptional analyses of reduced zein kernels derived from the opaque2 mutation and RNAi suppression.透明蛋白突变体和 RNAi 抑制导致的玉米醇溶蛋白减少型胚乳的组成和转录分析。
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Effects of floury-2 locus on zein accumulation and RNA metabolism during maize endosperm development.粉质2基因座对玉米胚乳发育过程中醇溶蛋白积累和RNA代谢的影响。
Biochem Genet. 1978 Feb;16(1-2):27-38. doi: 10.1007/BF00484382.
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A defective signal peptide in a 19-kD alpha-zein protein causes the unfolded protein response and an opaque endosperm phenotype in the maize De*-B30 mutant.玉米De*-B30突变体中19-kD α-醇溶蛋白的缺陷信号肽引发未折叠蛋白反应和不透明胚乳表型。
Plant Physiol. 2004 Jan;134(1):380-7. doi: 10.1104/pp.103.031310. Epub 2003 Dec 4.

引用本文的文献

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NAC-type transcription factors regulate accumulation of starch and protein in maize seeds.NAC 型转录因子调节玉米种子中淀粉和蛋白质的积累。
Proc Natl Acad Sci U S A. 2019 Jun 4;116(23):11223-11228. doi: 10.1073/pnas.1904995116. Epub 2019 May 20.
2
The ZmbZIP22 Transcription Factor Regulates 27-kD γ-Zein Gene Transcription during Maize Endosperm Development.ZmBZIP22 转录因子在玉米胚乳发育过程中调节 27-kD γ-Zein 基因的转录。
Plant Cell. 2018 Oct;30(10):2402-2424. doi: 10.1105/tpc.18.00422. Epub 2018 Sep 21.
3
The Maize Imprinted Gene Encodes a PLATZ Protein Required for tRNA and 5S rRNA Transcription through Interaction with RNA Polymerase III.玉米印迹基因编码一个 PLATZ 蛋白,该蛋白通过与 RNA 聚合酶 III 相互作用,参与 tRNA 和 5S rRNA 的转录。
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Transcriptional Regulation of Zein Gene Expression in Maize through the Additive and Synergistic Action of opaque2, Prolamine-Box Binding Factor, and O2 Heterodimerizing Proteins.通过不透明2、醇溶蛋白盒结合因子和O2异源二聚化蛋白的加性和协同作用对玉米醇溶蛋白基因表达的转录调控
Plant Cell. 2015 Apr;27(4):1162-72. doi: 10.1105/tpc.15.00035. Epub 2015 Apr 21.

本文引用的文献

1
Gamma-zeins are essential for endosperm modification in quality protein maize.γ-zeins 对于优质蛋白玉米胚乳的修饰是必不可少的。
Proc Natl Acad Sci U S A. 2010 Jul 20;107(29):12810-5. doi: 10.1073/pnas.1004721107. Epub 2010 Jul 6.
2
RNA interference-mediated change in protein body morphology and seed opacity through loss of different zein proteins.通过不同的醇溶蛋白缺失导致的蛋白体形态和种子不透明性的 RNA 干扰介导的变化。
Plant Physiol. 2010 May;153(1):337-47. doi: 10.1104/pp.110.154690. Epub 2010 Mar 17.
3
Non-Mendelian regulation and allelic variation of methionine-rich delta-zein genes in maize.玉米中富含蛋氨酸的δ-醇溶蛋白基因的非孟德尔调控及等位基因变异
Theor Appl Genet. 2009 Aug;119(4):721-31. doi: 10.1007/s00122-009-1083-5. Epub 2009 Jun 7.
4
Organization of the prolamin gene family provides insight into the evolution of the maize genome and gene duplications in grass species.醇溶蛋白基因家族的组织为了解玉米基因组的进化以及禾本科物种中的基因复制提供了线索。
Proc Natl Acad Sci U S A. 2008 Sep 23;105(38):14330-5. doi: 10.1073/pnas.0807026105. Epub 2008 Sep 15.
5
Subcellular structure of endosperm protein in high-lysine and normal corn.高赖氨酸玉米和普通玉米胚乳蛋白质的亚细胞结构
Science. 1967 Aug 4;157(3788):556-7. doi: 10.1126/science.157.3788.556.
6
Recent Linkage Studies in Maize.玉米近期的连锁研究。
Genetics. 1939 Jan;24(1):59-63. doi: 10.1093/genetics/24.1.59.
7
The maize Mucronate mutation is a deletion in the 16-kDa gamma-zein gene that induces the unfolded protein response.玉米具短尖突变是16 kDa γ-玉米醇溶蛋白基因中的一个缺失,它会引发未折叠蛋白反应。
Plant J. 2006 Nov;48(3):440-51. doi: 10.1111/j.1365-313X.2006.02884.x. Epub 2006 Sep 29.
8
A defective signal peptide in a 19-kD alpha-zein protein causes the unfolded protein response and an opaque endosperm phenotype in the maize De*-B30 mutant.玉米De*-B30突变体中19-kD α-醇溶蛋白的缺陷信号肽引发未折叠蛋白反应和不透明胚乳表型。
Plant Physiol. 2004 Jan;134(1):380-7. doi: 10.1104/pp.103.031310. Epub 2003 Dec 4.
9
Expression of a mutant alpha-zein creates the floury2 phenotype in transgenic maize.突变α-醇溶蛋白的表达在转基因玉米中产生粉质2表型。
Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):7094-7. doi: 10.1073/pnas.94.13.7094.
10
A defective signal peptide in the maize high-lysine mutant floury 2.玉米高赖氨酸突变体粉质2中的缺陷信号肽。
Proc Natl Acad Sci U S A. 1995 Jul 18;92(15):6828-31. doi: 10.1073/pnas.92.15.6828.

用 RNA 干扰拯救显性突变体。

Rescue of a dominant mutant with RNA interference.

机构信息

Waksman Institute of Microbiology, Rutgers University, Piscataway, New Jersey 08854, USA.

出版信息

Genetics. 2010 Dec;186(4):1493-6. doi: 10.1534/genetics.110.123471. Epub 2010 Sep 27.

DOI:10.1534/genetics.110.123471
PMID:20876558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2998327/
Abstract

Maize Mucronate1 is a dominant floury mutant based on a misfolded 16-kDa γ-zein protein. To prove its function, we applied RNA interference (RNAi) as a dominant suppressor of the mutant seed phenotype. A γ-zein RNAi transgene was able to rescue the mutation and restore normal seed phenotype. RNA interference prevents gene expression. In most cases, this is used to study gene function by creating a new phenotype. Here, we use it for the opposite purpose. We use it to reverse the creation of a mutant phenotype by restoring the normal phenotype. In the case of the maize Mucronate1 (Mc1) phenotype, interaction of a misfolded protein with other proteins is believed to be the basis for the Mc1 phenotype. If no misfolded protein is present, we can reverse the mutant to the normal phenotype. One can envision using this approach to study complex traits and in gene therapy.

摘要

玉米芒状突变体 1 是一种基于错误折叠的 16kDa γ-zein 蛋白的显性粉质突变体。为了证明其功能,我们应用 RNA 干扰(RNAi)作为突变体种子表型的显性抑制剂。γ-zein RNAi 转基因能够挽救突变并恢复正常种子表型。RNA 干扰可阻止基因表达。在大多数情况下,这是通过创建新表型来研究基因功能的。在这里,我们出于相反的目的使用它。我们使用它通过恢复正常表型来逆转突变体表型的产生。在玉米芒状突变体 1(Mc1)表型的情况下,人们认为错误折叠的蛋白质与其他蛋白质的相互作用是 Mc1 表型的基础。如果不存在错误折叠的蛋白质,我们可以将突变体逆转成正常表型。人们可以设想使用这种方法来研究复杂的特征和基因治疗。