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1
Organization of the Tgm family of transposable elements in soybean.大豆中转座元件Tgm家族的组织方式
Genetics. 1988 Oct;120(2):597-604. doi: 10.1093/genetics/120.2.597.
2
A putative autonomous 20.5 kb-CACTA transposon insertion in an F3'H allele identifies a new CACTA transposon subfamily in Glycine max.在一个F3'H等位基因中一个假定的自主20.5 kb - CACTA转座子插入鉴定出大豆中的一个新的CACTA转座子亚家族。
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The wp mutation of Glycine max carries a gene-fragment-rich transposon of the CACTA superfamily.大豆的wp突变携带一个富含基因片段的CACTA超家族转座子。
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The transposable element Tam1 from Antirrhinum majus shows structural homology to the maize transposon En/Spm and has no sequence specificity of insertion.来自金鱼草的转座元件Tam1与玉米转座子En/Spm具有结构同源性,且没有插入序列特异性。
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The endogenous transposable element Tgm9 is suitable for generating knockout mutants for functional analyses of soybean genes and genetic improvement in soybean.内源性转座元件Tgm9适用于生成大豆基因功能分析和大豆遗传改良的敲除突变体。
PLoS One. 2017 Aug 10;12(8):e0180732. doi: 10.1371/journal.pone.0180732. eCollection 2017.
2
Transposon Tagging of a Male-Sterility, Female-Sterility Gene, St8, Revealed that the Meiotic MER3 DNA Helicase Activity Is Essential for Fertility in Soybean.对雄性不育、雌性不育基因St8进行转座子标签分析发现,减数分裂MER3 DNA解旋酶活性对大豆育性至关重要。
PLoS One. 2016 Mar 1;11(3):e0150482. doi: 10.1371/journal.pone.0150482. eCollection 2016.
3
Methylation affects transposition and splicing of a large CACTA transposon from a MYB transcription factor regulating anthocyanin synthase genes in soybean seed coats.甲基化影响大豆种皮中一个调控花青素合酶基因的MYB转录因子的大型CACTA转座子的转座和剪接。
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4
A conserved zinc finger domain in higher plants.高等植物中一个保守的锌指结构域。
Plant Mol Biol. 1989 May;12(5):593-4. doi: 10.1007/BF00036972.
5
Unstable expression of a soybean gene during seed coat development.种子发育过程中大豆基因表达不稳定。
Theor Appl Genet. 1989 Apr;77(4):587-94. doi: 10.1007/BF00274285.
6
Germinal reversion of an unstable mutation for anthocyanin pigmentation in soybean.大豆花色素苷不稳定突变的生殖逆转。
Theor Appl Genet. 1990 Feb;79(2):161-7. doi: 10.1007/BF00225946.
7
Excision of an active CACTA-like transposable element from DFR2 causes variegated flowers in soybean [Glycine max (L.) Merr.].切除大豆 DFR2 中的一个活跃的 CACTA 类转座元件会导致花斑[Glycine max (L.) Merr.]。
Genetics. 2010 Jan;184(1):53-63. doi: 10.1534/genetics.109.107904. Epub 2009 Nov 6.
8
A putative autonomous 20.5 kb-CACTA transposon insertion in an F3'H allele identifies a new CACTA transposon subfamily in Glycine max.在一个F3'H等位基因中一个假定的自主20.5 kb - CACTA转座子插入鉴定出大豆中的一个新的CACTA转座子亚家族。
BMC Plant Biol. 2008 Dec 2;8:124. doi: 10.1186/1471-2229-8-124.
9
En/Spm-like transposons in Poaceae species: transposase sequence variability and chromosomal distribution.禾本科植物中的En/Spm样转座子:转座酶序列变异性和染色体分布
Cell Mol Biol Lett. 2006;11(2):214-30. doi: 10.2478/s11658-006-0017-3.
10
Transpositional behavior of the maize En/Spm element in transgenic tobacco.玉米 En/Spm 转座元件在转基因烟草中的转座行为。
EMBO J. 1989 May;8(5):1315-21. doi: 10.1002/j.1460-2075.1989.tb03511.x.

本文引用的文献

1
Highly structured sequence homology between an insertion element and the gene in which it resides.插入序列与位于其内的基因之间存在高度结构化的序列同源性。
Proc Natl Acad Sci U S A. 1985 Jan;82(2):493-7. doi: 10.1073/pnas.82.2.493.
2
Transcription of transposable element Activator (Ac) of Zea mays L.玉米转座因子 Activator(Ac)的转录
EMBO J. 1987 Jun;6(6):1555-63. doi: 10.1002/j.1460-2075.1987.tb02400.x.
3
The Spm (En) transposable element controls the excision of a 2-kb DNA insert at the wx allele of Zea mays.Spm(En)转座元件控制着玉米 wx 等位基因上 2kbDNA 插入片段的切除。
EMBO J. 1984 May;3(5):1021-8. doi: 10.1002/j.1460-2075.1984.tb01922.x.
4
The 17-kb Tam1 element of Antirrhinum majus induces a 3-bp duplication upon integration into the chalcone synthase gene.金鱼草的 17-kb Tam1 元件在整合到查尔酮合酶基因时会引起 3-bp 的重复。
EMBO J. 1984 May;3(5):1015-9. doi: 10.1002/j.1460-2075.1984.tb01921.x.
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Molecular analysis of the En/Spm transposable element system of Zea mays.玉米En/Spm转座子系统的分子分析。
EMBO J. 1986 May;5(5):835-41. doi: 10.1002/j.1460-2075.1986.tb04292.x.
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The making of strand-specific M13 probes.链特异性M13探针的制备。
Gene. 1982 Mar;17(3):271-7. doi: 10.1016/0378-1119(82)90143-3.
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cA lectin gene insertion has the structural features of a transposable element.一个C型凝集素基因插入具有转座元件的结构特征。
Cell. 1983 Oct;34(3):1023-31. doi: 10.1016/0092-8674(83)90560-3.
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An integrated and simplified approach to cloning into plasmids and single-stranded phages.一种整合且简化的克隆到质粒和单链噬菌体中的方法。
Methods Enzymol. 1983;101:78-89. doi: 10.1016/0076-6879(83)01006-x.
9
An insertion sequence blocks the expression of a soybean lectin gene.一个插入序列阻断了大豆凝集素基因的表达。
Cell. 1983 Jun;33(2):465-75. doi: 10.1016/0092-8674(83)90428-2.
10
The bidirectional transfer of DNA and RNA to nitrocellulose or diazobenzyloxymethyl-paper.DNA和RNA向硝酸纤维素或重氮苄氧基甲基纸的双向转移。
Anal Biochem. 1980 Nov 15;109(1):123-9. doi: 10.1016/0003-2697(80)90019-6.

大豆中转座元件Tgm家族的组织方式

Organization of the Tgm family of transposable elements in soybean.

作者信息

Rhodes P R, Vodkin L O

机构信息

Plant Genetics and Germplasm Institute, U.S. Department of Agriculture, Beltsville, Maryland 20705.

出版信息

Genetics. 1988 Oct;120(2):597-604. doi: 10.1093/genetics/120.2.597.

DOI:10.1093/genetics/120.2.597
PMID:2848748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1203536/
Abstract

We have compared the organization of six Tgm elements that were selected from a genomic library of soybean DNA on the basis of hybridization with subcloned regions of Tgm 1 (transposon, Glycine max) from the seed lectin gene. These elements ranged in size from 1.6 kbp to greater than 12 kbp. Tgm2, Tgm3, Tgm4 and Tgm5 represent partial isolates in which the genomic clone contained a 3' but not a 5' terminus of the element; while Tgm6 and Tgm7, like Tgm1, were small isolates flanked by both 5' and 3' nonelement sequences. Cross-hybridization studies between subcloned portions of these seven elements identified regions of homology which suggest that the Tgm transposable elements of soybean form a family of deletion derivatives. In addition to internal deletion events, numerous deletions and base substitutions are also present within the borders of these elements which are comprised of the same tandemly repeated sequence. The 39% amino acid homology between a 1 kb portion of an open reading frame in Tgm4 and Tgm5 and ORF1, an open frame from the first intron of the maize Enhancer (Suppressor-mutator) transposable element, suggests that both elements encode a common function that requires a high degree of protein conservation.

摘要

我们比较了从大豆DNA基因组文库中选出的6个Tgm元件的结构,这些元件是根据与种子凝集素基因的Tgm 1(转座子,大豆)亚克隆区域杂交而挑选出来的。这些元件大小从1.6千碱基对到大于12千碱基对不等。Tgm2、Tgm3、Tgm4和Tgm5代表部分分离株,其基因组克隆包含元件的3'端但不包含5'端;而Tgm6和Tgm7,与Tgm1一样,是两侧都有5'和3'非元件序列的小分离株。这七个元件亚克隆部分之间的交叉杂交研究确定了同源区域,这表明大豆的Tgm转座元件形成了一个缺失衍生物家族。除了内部缺失事件外,这些元件边界内还存在许多缺失和碱基替换,这些边界由相同的串联重复序列组成。Tgm4和Tgm5中一个1千碱基开放阅读框部分与玉米增强子(抑制-突变体)转座元件第一个内含子的开放框ORF1之间39%的氨基酸同源性表明,这两个元件都编码一种需要高度蛋白质保守性的共同功能。