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Clonal Fidelity of Micropropagated Psidium guajava L. Plants Using Microsatellite Markers

机译:使用微卫星标记的微繁殖番石榴番荔枝植物的克隆保真度

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Micropropagation of Psidium guajava L. (guava) is a viable alternative to currently adopted techniques for large-scale plant propagation of commercial cultivars. Assessment of clonal fidelity in micropropagated plants is the first step towards ensuring genetic uniformity in mass production of planting material. In the present study, 31 plants of guava cultivar “Lucknow 49” regenerated by micropropagation were tested for genetic fidelity by comparing them to the mother plant from which explant material was obtained. Efficient rooting of in vitro proliferated shoots was obtained by culture on 1/2 strength MS medium supplemented with either 9.8 μM indole butyric acid (IBA) or 11.4 μM indole acetic acid (IAA). Leaf samples of 31 regenerated plants were compared to the mother plant using 17 simple sequence repeat (SSR) markers. While 16 SSRs detected the same allele, locus mPgCIR07 detected slight differences, where six micropropagated plants were 1 bp smaller (152 bp) than the parental genotype (153 bp). Differences in leaf tissues for anthocyanin pigmentation were also noted among micropropagated plants. Results of the study indicated efficient rooting of “Lucknow-49” cultivar for rapid propagation of planting material, and revealed that micropropagated plants were identical for 16 of the 17 loci examined. Although most mutations induced by tissue culture may not have an effect on phenotype, the possibility that novel phenotypes can be generated in a commercial setting exists.
机译:番石榴(Pavadium guajava L.)(番石榴)的微繁殖是目前采用的商业化品种大规模植物繁殖技术的可行替代方法。微繁殖植物中克隆保真度的评估是确保种植材料大规模生产中遗传均匀性的第一步。在本研究中,将31种通过微繁繁殖的番石榴品种“勒克瑙49”的植物与获得外植体材料的母本植物进行了遗传保真度测试。通过在补充了9.8μM吲哚丁酸(IBA)或11.4μM吲哚乙酸(IAA)的1/2强度MS培养基上进行培养,可以获得体外增殖芽的有效生根。使用17个简单序列重复(SSR)标记将31个再生植物的叶子样品与母本植物进行比较。虽然16个SSRs检测到相同的等位基因,但基因座mPgCIR07检测到细微的差异,其中六种微繁殖的植物比亲本基因型(153 bp)小1 bp(152 bp)。在微繁殖的植物中,花色苷色素沉着的叶子组织也有所不同。研究结果表明,“ Lucknow-49”品种可有效生根以快速繁殖种植材料,并显示在所研究的17个基因座中,有16个基因的微繁殖植株相同。尽管由组织培养诱导的大多数突变可能对表型没有影响,但是存在可以在商业环境中产生新表型的可能性。

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