...
首页> 外文期刊>Acta Horticulturae >Physical mapping of 5S and 45S RDNAs by fluorescent in situ hybridization in mango ( Mangifera indica L.).
【24h】

Physical mapping of 5S and 45S RDNAs by fluorescent in situ hybridization in mango ( Mangifera indica L.).

机译:在芒果中通过荧光原位杂交技术对5S和45S RDNA进行物理定位。

获取原文
获取原文并翻译 | 示例
           

摘要

Mango (Mangifera indica L.) is thought to be diploid despite the many numbers of chromosomes (2n=2x=40). Although the allopolyploid nature of M. indica is reported by Mukherjee (1950), no chromosome studies are available to elucidate genome composition of mango until now. We have applied fluorescent in situ hybridization (FISH) technique using 5S and 45S ribosomal DNAs (rDNAs) as probes on the somatic metaphase chromosome of mango for the first step to elucidate genome composition of mango. The digoxigenin (DIG)-labeled 5S or 45S probe was hybridized onto the chromosomes separately, and both of them were visualized by incubation with anti-DIG-fluorescein isothiocyanate (FITC). Strong signals of 5S rDNA were observed on two chromosomes, and these two seemed to be homologous chromosomes due to their size and identical chromosomal location of 5S rDNA loci. On the other hand, six chromosomes were demonstrated to carry 45S rDNA loci. Among these six chromosomes, two chromosomes seemed to be homologous from their size and the location of rDNA loci in addition to signal intensity. But, another four chromosomes could not be identified whether or not these four form two pairs of chromosomes, since no clear images of these chromosomes were observed. In addition, multicolor FISH using 5S and 45S rDNA probes differently labeled with DIG and biotin, revealed separate localization of the two rDNA genes on different chromosomes of mango. We could distinguish eight chromosomes among forty chromosomes of mango in this study, but no evidence was obtained for a possibility of heterozygotic karyotype in mango not like in sweet orange.
机译:尽管有许多染色体(2 n = 2 x = 40),但芒果(Mangifera indica L.)被认为是二倍体。尽管 M的同质多倍体性质。印度是由穆克吉(Mukherjee,1950年)报道的,迄今为止尚无染色体研究来阐明芒果的基因组组成。我们已经应用荧光原位杂交(FISH)技术,使用5S和45S核糖体DNA(rDNA)作为芒果体细胞中期染色体上的探针,以阐明芒果的基因组组成。将洋地黄毒苷(DIG)标记的5S或45S探针分别杂交到染色体上,并通过与异硫氰酸抗DIG荧光素(FITC)孵育来可视化它们。在两个染色体上观察到5S rDNA的强信号,由于这两个染色体的大小和5S rDNA基因座的染色体位置相同,它们似乎是同源染色体。另一方面,证明了六个染色体带有45S rDNA基因座。在这六个染色体中,除了信号强度外,还有两个染色体在大小和rDNA基因座位置上似乎是同源的。但是,由于没有观察到这些染色体的清晰图像,因此无法识别出这四个染色体是否形成了两对染色体。此外,使用5S和45S rDNA探针分别用DIG和生物素标记的多色FISH,揭示了两个rDNA基因在芒果不同染色体上的独立定位。在这项研究中,我们可以在芒果的40条染色体中区分出8条染色体,但是没有证据表明芒果中的杂合核型可能不同于甜橙。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号