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A helitron-like transposon superfamily from lepidoptera disrupts (GAAA)(n) microsatellites and is responsible for flanking sequence similarity within a microsatellite family

机译:鳞翅目的直升机类超直升机转座子超家族破坏了(GAAA)(n)微卫星,并负责微卫星家族内侧翼序列的相似性

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摘要

Transposable elements (TEs) are mobile DNA regions that alter host genome structure and gene expression. A novel 588 bp non-autonomous high copy number TE in the Ostrinia nubilalis genome has features in common with miniature inverted-repeat transposable elements (MITEs): high A + T content (62.3%), lack of internal protein coding sequence, and secondary structure consisting of subterminal inverted repeats (SIRs). The O. nubilalis TE has inserted at (GAAA)n microsatellite loci, and was named the microsatellite-associated interspersed nuclear element ( MINE-1). Non-autonomous MINE-1 superfamily members also were identified downstream of (GAAA)n microsatellites within Bombyx mori and Pectinophora gossypiella genomes. Of 316 (GAAA)n microsatellites from the B. mori whole genome sequence, 201 (63.6%) have associated autonomous or non-autonomous MINE-1 elements. Autonomous B. mori MINE-1s a encode a helicase and endonuclease domain RepHel-like protein (BMHELp1) indicating their classification as Helitron-like transposons and were renamed Helitron1_BM. Transposition of MINE-1 members in Lepidoptera has resulted in the disruption of (GAAA)n microsatellite loci, has impacted the application of microsatellite-based genetic markers, and suggests genome sequence that flanks TT/AA dinucleotides may be required for target site recognition by RepHel endonuclease domains.
机译:转座因子(TEs)是可移动的DNA区域,可改变宿主基因组结构和基因表达。 Ostrinia nubilalis基因组中新的588 bp非自治高拷贝数TE具有与微型反向重复转座因子(MITE)相同的特征:高A + T含量(62.3%),内部蛋白编码序列不足和次级由亚末端反向重复序列(SIR)组成的结构。 O.nubilalis TE已插入(GAAA)n微卫星基因座,并被命名为与微卫星相关的散布式核元件(MINE-1)。非自主的MINE-1超家族成员也被确定在家蚕和果蝇果蝇基因组内(GAAA)n微卫星的下游。在来自桑蚕芽孢杆菌全基因组序列的316个(GAAA)n微卫星中,有201个(63.6%)具有相关的自治或非自治MINE-1元件。自主桑蚕MINE-1s编码解旋酶和核酸内切酶结构域RepHel样蛋白(BMHELp1),表明它们被分类为Helitron样转座子,并被重命名为Helitron1_BM。鳞翅目中MINE-1成员的转座导致(GAAA)n微卫星基因座的破坏,影响了基于微卫星的遗传标记的应用,并暗示了TT / AA二核苷酸侧翼的基因组序列可能需要通过RepHel核酸内切酶结构域。

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