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[小麦MIR156前体基因的克隆及小麦miR156靶向的TaSPL17的序列多态性]

[Cloning of tae-MIR156 precursor gene and sequence polymorphisms of tae-miR156 targeted TaSPL17].

作者信息

Xia Liu, Bin Zhang, Xinguo Mao, Ang Li, Meirong Sun, Ruilian Jing

机构信息

College of Bioengineering, Shanxi University, Taiyuan 030006, China; National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China;

National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

出版信息

Yi Chuan. 2014 Jun;36(6):592-602. doi: 10.3724/SP.J.1005.2014.0592.

Abstract

Squamosa-promoter binding protein (SBP)-box genes, encoding plant-specific transcription factors, play an important role in plant development. Some members of the SBP-box gene family are regulated by miR156. In this study, we cloned the tae-MIR156 precursor gene, which could form a stem loop after its transcription. Sequence analysis showed that TaSPL3 and TaSPL17 had putative targets of tae-miR156 among the ten wheat SBP-box genes. The diploid donor species of hexaploid common wheat (Triticum aestivum, genome AABBDD), i.e., Triticum urartu (AA) UR209 and Aegilops speltoides Y2001 (SS, closely related to BB) possessed more than one copy of SPL17 (SPL17-A1, SPL17-A2 and SPL17-A3 from Triticum urartu; SPL17-B1, SPL17-B2 and SPL17-B3 from Aegilops speltoides), while Aegilops tauschii (DD) Ae38 only possessed one (SPL17-D). The identities between nucleotide sequences of SPL17-A2 and SPL17-B2, SPL17-A3 and SPL17-B3 or SPL17-D were higher than 99%. They were highly similar with the sequence of TaSPL17 in common wheat cultivars Chinese Spring, Hengguan 35 and Shuangfengshou. These genes might originate from a common ancestor and were highly conserved in the process of evolution. The target site of tae-miR156 in TaSPL17 was also highly conserved in two subgroups consisted of accessions with diverse spike number per plant and genetic background.

摘要

编码植物特异性转录因子的Squamosa启动子结合蛋白(SBP)盒基因在植物发育中起重要作用。SBP盒基因家族的一些成员受miR156调控。在本研究中,我们克隆了tae-MIR156前体基因,其转录后可形成茎环结构。序列分析表明,在十个小麦SBP盒基因中,TaSPL3和TaSPL17具有tae-miR156的推定靶标。六倍体普通小麦(Triticum aestivum,基因组AABBDD)的二倍体供体物种,即乌拉尔图小麦(AA)UR209和斯卑尔脱山羊草Y2001(SS,与BB密切相关)拥有多个SPL17拷贝(来自乌拉尔图小麦的SPL17-A1、SPL17-A2和SPL17-A3;来自斯卑尔脱山羊草的SPL17-B1、SPL17-B2和SPL17-B3),而节节麦(DD)Ae38仅拥有一个(SPL17-D)。SPL17-A2与SPL17-B2、SPL17-A3与SPL17-B3或SPL17-D的核苷酸序列同一性高于99%。它们与普通小麦品种中国春、衡观35和双峰寿中TaSPL17的序列高度相似。这些基因可能起源于一个共同祖先,并且在进化过程中高度保守。TaSPL17中tae-miR156的靶位点在由单株穗数和遗传背景不同的材料组成的两个亚组中也高度保守。

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