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Cloning and Characterization of ThSHRs and ThSCR Transcription Factors in Taxodium Hybrid ‘Zhongshanshan 406’

机译:杂交种中山山406中ThSHRs和ThSCR转录因子的克隆与鉴定

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摘要

Among the GRAS family of transcription factors, SHORT ROOT (SHR) and SCARECROW (SCR) are key regulators of the formation of root tissues. In this study, we isolated and characterized two genes encoding SHR proteins and one gene encoding an SCR protein: ThSHR1 (Accession Number ), ThSHR2 (Accession Number ) and ThSCR (Accession Number ) in the adventitious roots of Taxodium hybrid ‘Zhongshanshan’. Gene structure analysis indicated that ThSHR1, ThSHR2 and ThSCR are all intron free. Multiple protein sequence alignments showed that each of the corresponding proteins, ThSHR1, ThSHR2 and ThSCR, contained five well-conserved domains: leucine heptad repeat I (LHRI), the VHIID motif, leucine heptad repeat II (LHR II), the PFYRE motif, and the SAW motif. The phylogenetic analysis indicated that ThSCR was positioned in the SCR clade with the SCR proteins from eight other species, while ThSHR1 and ThSHR2 were positioned in the SHR clade with the SHR proteins from six other species. Temporal expression patterns of these genes were profiled during the process of adventitious root development on stem cuttings. Whereas expression of both ThSHR2 and ThSCR increased up to primary root formation before declining, that of ThSHR1 increased steadily throughout adventitious root formation. Subcellular localization studies in transgenic poplar protoplasts revealed that ThSHR1, ThSHR2 and ThSCR were localized in the nucleus. Collectively, these results suggest that the three genes encode Taxodium GRAS family transcription factors, and the findings contribute to improving our understanding of the expression and function of SHR and SCR during adventitious root production, which may then be manipulated to achieve high rates of asexual propagation of valuable tree species.
机译:在GRAS转录因子家族中,SHORT ROOT(SHR)和SCARECROW(SCR)是根组织形成的关键调控因子。在这项研究中,我们分离和鉴定了两种编码SHR蛋白的基因和一个编码SCR蛋白的基因:ThSHR1(登录号),ThSHR2(登录号)和ThSCR(登录号)位于紫杉属杂种“中山山”的不定根中。基因结构分析表明,ThSHR1,ThSHR2和ThSCR均不含内含子。多个蛋白质序列比对显示,每个相应的蛋白质ThSHR1,ThSHR2和ThSCR包含五个保守性良好的结构域:亮氨酸七肽重复序列I(LHRI),VHIID基序,亮氨酸七肽重复序列II(LHR II),PFYRE基序,和SAW主题。系统发育分析表明,ThSCR和其他八个物种的SCR蛋白一起位于SCR进化枝中,而ThSHR1和ThSHR2与其他六个物种的SHR蛋白质一起位于SHR进化枝中。这些基因的时间表达模式在茎插条不定根发育过程中进行了分析。尽管ThSHR2和ThSCR的表达在下降之前一直增加到主要根系的形成,而ThSHR1的表达在整个不定根形成过程中均稳定地增加。转基因杨树原生质体中的亚细胞定位研究表明,ThSHR1,ThSHR2和ThSCR定位在细胞核中。总的来说,这些结果表明,这三个基因编码了Taxodium GRAS家族转录因子,这些发现有助于提高我们对不定根产生过程中SHR和SCR表达和功能的了解,然后可以对其进行操纵以实现无性繁殖的高比率。的珍贵树种。

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