Sahoo Pragnya, Jena Satyanarayan, Mohanty Suprava, Das Anath Bandhu
Cytogenetics Laboratory, Regional Plant Resource Centre, Nayapalli, Bhubaneswar-751015, Orissa, India.
Rev Biol Trop. 2007 Jun;55(2):437-48. doi: 10.15517/rbt.v55i2.6023.
Analysis of karyotype, nuclear DNA content and RAPD markers were performed in four species of Bruguiera (Rhizophoraceae) of Bhitarkanika mangrove forests, Orissa, India. Detailed karyotype analysis revealing 2n=34 in B. cylindrica and 2n=36 in B. gymnorrhiza was reported for the first time and 2n=34 in B. parviflora and B. sexangula was confirmed. On the basis of the common types of chromosomes present among Bruguiera, two distinct groups were found; one consists of B. cylindrica and B. parviflora and the other of B. gymnorrhiza and B. sexangula. The symmetrical karyotype with same chromosome types grouped B. cylindrica and B. parviflora together and presence of Type E chromosomes placed B. gymnorrhiza and B. sexangula in a separate group, suggesting their closer affinity in their respective group. Analysis of chromosome length, volume, INV and 4C DNA content confirmed this division. Nuclear DNA content was two-fold higher (approximately 17.0 pg) in the second group than in the first (approximately 8.0 pg). The amplification products generated through RAPD revealed 1-9 amplicons with size variations from 600 bp to 2 500 bp with 49.31% genetic similarity between B. gymnorrhiza and B. sexangula and 47.10% in between B. cylindrica and B. parviflora. The high copy number marker band (approximately 1,100 bp) yielded in OPN-15 primer in B. parviflora the characteristic DNA marker, which was cloned and used as probes for assessment of genetic diversity, and demonstrated its close genetic affinity to B. cylindrica. B. gymnorrhiza and B. sexangula also produced similar marker bands of approximately 600 bp and approximately 2,200 bp in the same primer. All of the cytological, 4C DNA content and RAPD data confirmed the existence of two taxonomically distinct groups of Bruguiera: one consisting of B. cylindrica and B. parviflora and the other of B. gymnorrhiza and B. sexangula as placed earlier (1862) in the tribe Rhizophoreae by Bentham and Hooker, on the basis of the flowering habits ofBruguiera. Genetically, the B. sexangula and B. gymnorrhiza group was found to be very closely, rather than distantly, related to B. parviflora and B. cylindrica. Our results demonstrate that molecular markers together with cytological evidence provide an effective tool to access the existing interspecific genetic polymorphism in mangrove species, to solve the taxonomic problems and to design their conservation strategy.
对印度奥里萨邦比塔尔卡尼卡红树林的四种木榄属(红树科)植物进行了核型、核DNA含量和随机扩增多态性DNA(RAPD)标记分析。首次详细报道了柱果木榄的核型分析结果为2n = 34,木榄为2n = 36,小花木榄和海莲2n = 34也得到确认。根据木榄属植物中常见的染色体类型,发现了两个不同的类群;一个类群由柱果木榄和小花木榄组成,另一个由木榄和海莲组成。具有相同染色体类型的对称核型将柱果木榄和小花木榄归为一组,E型染色体的存在将木榄和海莲归为另一组,表明它们在各自类群中亲缘关系更近。染色体长度、体积、臂比和4C DNA含量分析证实了这种分类。第二组的核DNA含量(约17.0 pg)比第一组(约8.0 pg)高出两倍。通过RAPD产生的扩增产物显示,有1 - 9个扩增片段,大小在600 bp至2500 bp之间变化,木榄和海莲之间的遗传相似性为49.31%,柱果木榄和小花木榄之间为47.10%。小花木榄中由OPN - 15引物产生的高拷贝数标记带(约1100 bp)产生了特征性DNA标记,该标记被克隆并用作评估遗传多样性的探针,结果表明它与柱果木榄有密切的遗传亲缘关系。木榄和海莲在同一引物中也产生了类似的约600 bp和约2200 bp的标记带。所有的细胞学、4C DNA含量和RAPD数据都证实了木榄属存在两个分类学上不同的类群:一个由柱果木榄和小花木榄组成,另一个由木榄和海莲组成,这与边沁和胡克于1862年根据木榄的开花习性将其归入红树族时的分类一致。从遗传学角度来看,海莲和木榄类群与小花木榄和柱果木榄的关系非常密切,而非疏远。我们的结果表明,分子标记与细胞学证据相结合,为了解红树林物种现有的种间遗传多态性、解决分类学问题以及设计保护策略提供了一种有效的工具。