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分析与油菜籽发育相关基因的差异表达。

Analysis of the differential expression of the genes related to Brassica napus seed development.

机构信息

Department of Bioengineering, Zhengzhou University, 450001, Zhengzhou, China.

出版信息

Mol Biol Rep. 2011 Feb;38(2):1055-61. doi: 10.1007/s11033-010-0202-3. Epub 2010 Jun 23.

Abstract

To screen the genes related to Brassica napus seed development at pattern formation and maturation stages, the suppression subtractive cDNA libraries of B. napus cultivar Zhongshuang 6 were constructed with its embryos at 10 days after flowering (10 DAF) and 30 days after flowering (30 DAF) through suppression subtractive hybridization (SSH) technology. The positive clones were screened by PCR and dot blot hybridization, and then sequenced. High quality expressed sequence tags (ESTs) were used for COG functional classification with COGNITOR software, as well as analysis and annotation with BLAST software. Tissue-specific detection of five genes screened was performed by RT-PCR in root, stem, leaf, flower, bud, pod, and embryo tissues. The insert size ranged from 100 to 900 bp, with an average size of about 500 bp. According to COG functional classification database, the differentially expressed genes mainly involved in lipid and amino acid metabolism, signal transduction, post-transcriptional modification, and etc. The results from RT-PCR detection of the five differentially expressed genes indicated that genes 2-96 and 2-352 presented embryo-specific expression, gene 1-385 expressed in parts of tissues, and genes 1-71 and 1-682 expressed in all tissues. Two genes were found to be involved in seed development, lipid and protein metabolisms, two genes may be involved in signal transduction, one gene could not match with the homologous sequences known to date and was likely a new gene. These results are helpful for future gene cloning and their functional analysis.

摘要

为了筛选甘蓝型油菜种子发育相关基因在形态发生和成熟阶段,通过抑制差减杂交(SSH)技术构建了中双 6 号油菜品种胚胎在开花后 10 天(10 DAF)和开花后 30 天(30 DAF)的抑制消减 cDNA 文库。通过 PCR 和点杂交筛选阳性克隆,然后测序。使用 COGNITOR 软件对高质量表达序列标签(EST)进行 COG 功能分类,并用 BLAST 软件进行分析和注释。通过 RT-PCR 在根、茎、叶、花、芽、荚和胚胎组织中对筛选出的 5 个基因进行组织特异性检测。插入片段大小从 100 到 900 bp 不等,平均大小约为 500 bp。根据 COG 功能分类数据库,差异表达基因主要涉及脂质和氨基酸代谢、信号转导、转录后修饰等。5 个差异表达基因的 RT-PCR 检测结果表明,基因 2-96 和 2-352 呈现胚胎特异性表达,基因 1-385 在部分组织中表达,基因 1-71 和 1-682 在所有组织中表达。发现两个基因参与种子发育和脂质及蛋白质代谢,两个基因可能参与信号转导,一个基因与目前已知的同源序列不匹配,可能是一个新基因。这些结果有助于未来的基因克隆及其功能分析。

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