Identification of different cDNA clones of the Apomixis-specific gene-1 homolog involved in aposporous embryo sac formation in guineagrass (Panicum maximum Jacq.).

IF 1.4 4区 生物学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Lanzhuang Chen, Liming Guan, Taiji Adachi
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引用次数: 0

Abstract

Apomixis is the reproduction mode in which only the mother's genes are transmitted from generation to generation. If this trait can be put to practical use, it is expected to be a truly epoch-making breeding method, as seed production costs can be greatly reduced by fixing F1 hybrids. This study aimed to isolate the aposporous apomixis gene and analyze how the gene(s) will be expressed from/in the aposporous guineagrass (Panicum maximum Jacq.). A new classification method using the ovary length as an index was developed to sample different developmental stages of ovaries and buds in obligate sexual plants and apomicts. A cDNA library was derived from the ovaries of aposporous accession N68/96-8-o-11 staged at the appearance of aposporous initial cells (AICs) to isolate AIC stage-specific genes. Using differential screening, four AIC stage-specific cDNA clones obtained from ten thousand of plaques by Northern blot hybridization showed the same start codon and sequences, ranging in lengths from 577 to 1182 bp. The characteristics and their homologies of the four cDNA clones are similar to Apomixis-specific gene-1 (ASG-1), indicating that they are the different cDNA clones of Apomixis-specific gene-1 homolog (ASG-1H). In situ expression analysis detected signals without distinguishing between ASG-1 mRNA and the ASG-1H on gene expression specifically in AIC, AIC-derived embryo sacs, and root tips and shoot apical meristems of aposporous accession. The finding and identification of ASG-1H expressed at the times of AIC appearance and AIC-derived embryo sac formation, may represent an initial step towards isolating an apospory gene.

豚草无孢子胚囊形成的无融合特异性基因-1同源基因cDNA克隆的鉴定。
无融合是一种只有母亲的基因代代相传的繁殖方式。如果该性状能够投入实际应用,通过固定F1杂交种可以大大降低制种成本,有望成为一种真正划时代的育种方法。本研究旨在分离无孢子无融合基因,并分析该基因如何在无孢子豚草(Panicum maximum Jacq.)中表达。提出了一种以子房长度为指标对专性植物和单性植物的子房和芽的不同发育阶段进行分类的新方法。从无孢子入种n68 /96-8- 0 -11的子房中获得了一个cDNA文库,以分离无孢子初始细胞(AIC)出现时的AIC阶段特异性基因。通过差异筛选,从10000个斑块中获得的4个AIC阶段特异性cDNA克隆显示相同的起始密码子和序列,长度从577到1182 bp不等。4个cDNA克隆的特征及其同源性与无融合性特异性基因-1 (Apomixis-specific gene-1, ASG-1)相似,表明它们是无融合性特异性基因-1同源物(Apomixis-specific gene-1 homolog - 1h)的不同cDNA克隆。原位表达分析检测到不区分ASG-1 mRNA和ASG-1H的基因表达信号,特别是在AIC、AIC衍生胚囊和无孢子加入的根尖和茎尖分生组织中。在AIC出现和AIC衍生的胚囊形成时表达的ASG-1H的发现和鉴定可能代表了分离apospory基因的第一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plant Biotechnology
Plant Biotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-PLANT SCIENCES
CiteScore
2.90
自引率
18.80%
发文量
45
审稿时长
6-12 weeks
期刊介绍: Plant Biotechnology is an international, open-access, and online journal, published every three months by the Japanese Society for Plant Biotechnology. The journal, first published in 1984 as the predecessor journal, “Plant Tissue Culture Letters” and became its present form in 1997 when the society name was renamed to Japanese Society for Plant Cell and Molecular Biology, publishes findings in the areas from basic- to application research of plant biotechnology. The aim of Plant Biotechnology is to publish original and high-impact papers, in the most rapid turnaround time for reviewing, on the plant biotechnology including tissue culture, production of specialized metabolites, transgenic technology, and genome editing technology, and also on the related research fields including molecular biology, cell biology, genetics, plant breeding, plant physiology and biochemistry, metabolic engineering, synthetic biology, and bioinformatics.
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