4.4 Article

The chromosomal constitution of fish hybrid lineage revealed by 5S rDNA FISH

期刊

BMC GENETICS
卷 16, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12863-015-0295-8

关键词

Interspecific hybridization; Heterozygous chromosomes; FISH; 5S rDNA

资金

  1. National Natural Science Foundation of China [30901100/31430088]
  2. Cooperative Innovation Center of Engineering and New Products for Developmental Biology of Hunan Province [20134486]
  3. major international cooperation projects of the National Natural Science Foundation of China [31210103918]
  4. training Program of the Major Research Plan of the National Natural Science Foundation of China [91331105]
  5. National High Technology Research and Development Program of China [2011AA100403]
  6. National Key Basic Research Program of China [2012CB722305]
  7. fund of education department of Hunan province [15A116]
  8. fund of sci-tec innovation and entrepreneur for Hunan young talents
  9. Science and Technology Program of Hunan Province [2015JC3065, 2014FJ3084]
  10. construct program of the key discipline in Hunan province and China

向作者/读者索取更多资源

Background: The establishment of the bisexual fertile fish hybrid lineage including the allodiploid and allotetraploid hybrids, from interspecific hybridization of red crucian carp (Carassius auratus red var. 2n = 100, 2n = AA) (female) x common carp (Cyprinus carpio L. 2n = 100, 2n = BB) (male), provided a good platform to investigate genetic relationship between the parents and their hybrid progenies. Results: The chromosomal inheritance of diploid and allotetraploid hybrid progenies in successive generations, was studied by applying 5S rDNA fluorescence in situ hybridization. Signals of 5S rDNA distinguished the chromosomal constitution of common carp (B-genome) from red crucian carp (A-genome), in which two strong signals were observed on the first submetacentric chromosome, while no major signal was found in common carp. After fish hybridization, one strong signal of 5S rDNA was detected in the same locus on the chromosome of diploid hybrids. As expected, two strong signals were observed in 4nF(3) tetraploid hybrids offspring and it is worth mentioning that two strong signals were detected in a separating bivalent of a primary spermatocyte in 4nF(3). Furthermore, the mitosis of heterozygous chromosomes was shown normal and stable with blastular tissue histological studies. Conclusions: We revealed that 5S rDNA signal can be applied to discern A-genome from B-genome, and that 5S rDNA bearing chromosomes can be stably passed down in successive generations. Our work provided a significant method in fish breeding and this is important for studies in fish evolutionary biology.

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