Abnormal chromosome behavior during meiosis in the allotetraploid of Carassius auratus red var. (♀) × Megalobrama amblycephala(♂)
© Qin et al.; licensee BioMed Central Ltd. 2014
Received: 26 April 2014
Accepted: 21 August 2014
Published: 2 September 2014
Allopolyploids generally undergo bivalent pairing at meiosis because only homologous chromosomes pair up. On the other hand, several studies have documented abnormal chromosome behavior during mitosis and meiosis in allopolyploids plants leading to the production of gametes with complete paternal or maternal chromosomes. Polyploidy is relatively rare in animals compared with plants; thus, chromosome behavior at meiosis in the allopolyploid animals is poorly understood.
Tetraploid hybrids (abbreviated as 4nRB) (4n = 148, RRBB) of Carassius auratus red var. (abbreviated as RCC) (2n = 100, RR) (♀) × Megalobrama amblycephala (abbreviated as BSB) (2n = 48, BB) (♂) generated gametes of different size. To test the genetic composition of these gametes, the gynogenetic offspring and backcross progenies of 4nRB were produced, and their genetic composition were examined by chromosome analysis and FISH. Our results suggest that 4nRB can produce several types of gametes with different genetic compositions, including allotetraploid (RRBB), autotriploid (RRR), autodiploid (RR), and haploid (R) gametes.
This study provides direct evidence of abnormal chromosome behavior during meiosis in an allotetraploid fish.
Polyploids are reported in plants, fish and amphibians, and are usually fit and well adapted ,. Most polyploids have an even number of chromosomes sets, with four being the most common (tetraploidy). Allopolyploids result from the combination of chromosome sets from two or more different taxa that undergo bivalent pairing at meiosis because only homologous chromosomes pair up ,. It is important that a diploid-like pairing system prevents meiotic irregularities and improves the efficiency of gamete production in allopolyploid species .
Allopolyploid speciation can result from chromosome doubling in a diploid hybrid to create unreduced gametes. When these diploid eggs and sperm are fertilized, they produce a tetraploid ,. In our previous study, the tetraploid (abbreviated as 4nRB) (4n = 148, RRBB) was obtained in the first generation of Carassius auratus red var. (abbreviated as RCC) (2n = 100, RR) (♀) × Megalobrama amblycephala (abbreviated as BSB) (2n = 48, BB) (♂), and resulted from the inhibition of the first cleavage of the fertilized eggs [8-10]. In this study, we provide direct evidence that abnormal chromosome behavior during meiosis occur in the allotetraploid hybrids, but bivalent pairing and the mechanisms of the abnormal chromosome behavior need to be investigated in future. This is the first report of abnormal chromosome behavior during meiosis in allotetraploid fish, and will contribute to the understanding of vertebrate polyploidization and evolution.
All samples were cultured in ponds at the Protection Station of Polyploidy Fish, Hunan Normal University, and fed with artificial feed. Fish treatments were carried out according to the regulations for protected wildlife and the Administration of Affairs Concerning Animal Experimentation, and approved by the Science and Technology Bureau of China. Approval from the Department of Wildlife Administration was not required for the experiments conducted in this paper. The fish were deeply anesthetized with 100 mg/L MS-222 (Sigma-Aldrich, St Louis, MO, USA) before dissection.
During the reproductive seasons (April to June) in 2004, 2005, and 2006, 4nRB of RCC (♀) × BSB (♂) were produced. During the reproductive seasons of 2006 and 2007, gynogenetic offspring (G-1, G-2, G-3) were obtained by artificial gynogenesis from 4nRB eggs that were activated with UV-treated sterilized BSB sperm, without chromosomes doubling treatment. During the reproductive season of 2008, the backcross progenies (H-1, H-2, H-3) of 4nRB (♀) × RCC (♂) were produced.
The semen of 4nRB was collected with a clean pipette and transferred into 2.5% glutaraldehyde solution. The semen was centrifuged at 2000 r/min for 1 min, fixed in 4% glutaraldehyde solution overnight, and then fixed in 1% osmic acid solution for 2 h. The spermatozoa were dehydrated in alcohol, dropped onto slides, desiccated, coated atomized gold, and then observed with an X-650 (Hitachi) SEM scan-electron micro-scope.
Preparation of chromosome spreads
To determine ploidy, chromosome counts were performed using kidney tissue from 10 individuals each of RCC, BSB, G-1, G-2, G-3, H-1, H-2, and H-3 at 1 year of age. After culture for 1-3 d at a water temperature of 18-22°C, the samples were injected with concanavalin one to three times at a dose of 2-8 mg/g body weight. The interval between injections was 12-24 h. Six hours prior to dissection each sample was injected with colchicine at a dose of 2-4 mg/g body weight. The kidney tissue was ground in 0.9% NaCl, followed by hypotonic treatment with 0.075 m KCl at 37°C for 40-60 min and then fixed in 3:1 methanol-acetic acid with three changes. The cells were dropped onto cold, wet slides and stained for 30 min in 4% Giemsa. The shape and number of chromosomes were analyzed under a microscope. For each type of fish, 200 metaphase spreads (20 metaphase spreads from each sample) of chromosomes were analyzed. The preparations were examined under an oil lens at a magnification of 3330 ×.
Fluorescence in situhybridization
Species-specific centromere probes of fluorescence in situ hybridization (FISH) were made from RCC and amplified by PCR using the primers 5′-TTCGAAAAGAGAGAATAATCTA-3′ and 5′-AACTCGTCTAAACCCGAACTA-3′. The FISH probes were produced by Dig-11-dUTP labeling (using a nick translation kit, Roche, Germany) of purified PCR products. FISH was performed according to He et al. . For each type of fish, 200 metaphase chromosome spreads from 10 individuals were analyzed under a Leica inverted CW4000 microscope with a Leica LCS SP2 confocal imaging system (Leica, Germany). Captured images were colored and overlapped in Adobe Photoshop CS6.
The size of gametes produced by 4nRB
Formation of gynogenetic and backcross progenies
Examination of chromosome number
Examination of chromosome number in RCC, BSB, 4nRB, gynogenetic offspring (G-1, G-2, and G-3) and backcross progenies (H-1, H-2, and H-3) of 4nRB
No. of metaphase
Distribution of chromosome number
Fluorescence in situ hybridization
Examination of hybridizing signals by FISH in RCC, BSB, the gynogenetic offspring (G-1, G-2, and G-3) and backcross progenies (H-1, H-2, and H-3) of 4nRB
No. of fish
No. of metaphase
Distribution of chromosome loci number
Generally, the pairing of homologous chromosomes is defective in the F1 hybrids because of divergence in the structure and number of chromosomes . However, the F1 hybrids can generate unreduced gametes by chromosome doubling; thus, they can produce allotetraploid offspring after fertilization of the diploid eggs and sperm from females and males of the diploid hybrid. This produces an allotetraploid in which the two homologous chromosome sets pair independently and allodiploid gametes are created ,,. In our previous study, allotetraploid hybrids (4nRB, 4n = 148, RRBB) were obtained in the first generation of RCC (2n = 100, RR, ♀) × BSB (2n = 48, BB, ♂), and possessed two sets of RCC-derived chromosomes and two sets of BSB-derived chromosomes ,. Theoretically, the two homologous chromosomes sets should pair independently, and thus bring about diploid-like meiotic behavior in 4nRB to produce allodiploid gametes (2n = 74, RB). However, the genetic composition of gamete indicated the surprising proof of abnormal chromosome behavior during meiosis in 4nRB.
In this paper, gynogenetic offspring (G-1, G-2, and G-3) were obtained by artificial gynogenesis, from 4nRB eggs that were activated with UV-treated sterilized sperm of BSB (2n = 48) but not subjected to chromosome doubling treatment (Figure 2C). The backcross progenies (H-1, H-2, and H-3) of 4nRB (♀) × RCC (♂) were then produced (Figure 2B). We evaluated the genetic composition of the gynogenetic offspring and backcross progenies by analyzing chromosome numbers and loci to infer chromosome behavior during meiosis in 4nRB, including the ploidy level and genetic composition of the gametes. For the gynogenetic offspring, our results suggested that G-1 (2n = 100, RR) were autodiploids with two sets of RCC-derived chromosomes (Figure 3A; Figure 4C), G-2 (4n = 148, RRBB) were allotetraploid with two sets of RCC-derived chromosomes and two sets of BSB-derived chromosomes (Figure 3B; Figure 4D), and G-3 (3n = 150, RRR) were autotriploids with three sets of RCC-derived chromosomes (Figure 3C; Figure 4E). Thus, these results provide direct proof of that 4nRB can produce many gametes with different genetic compositions, including allotetraploid (RRBB), autotriploid (RRR), and autodiploid (RR) gamete. In the backcross progenies, H-1 were autodiploids with two sets of RCC-derived chromosomes (Figure 3D; Figure 4F), suggesting that 4nRB can produce the haploid gamete (R). H-2 were autotriploids with three sets of RCC-derived chromosomes (Figure 3E; Figure 4G), suggesting that 4nRB can produce the autodiploid gametes (RR). Finally, H-3 (5n = 198, RRRBB) were allopentaploids with three sets of RCC-derived chromosomes and two sets of BSB-derived chromosomes (Figure 3F; Figure 4H), suggesting that 4nRB can produce the allotetraploid gametes (RRBB).
In 1935, the separation of parental genomes during mitotic and meiotic divisions of hybrid cells was firstly proposed in sexual hybrids between cultivated Brassica species . Until now, several studies have documented abnormal chromosome behavior during mitosis and meiosis in allopolyploids that leads to the production of gametes with complete paternal or maternal chromosomes [13-15]. In this paper, 4nRB produce several types of gametes with different genetic compositions, including allotetraploid (RRBB), autotriploid (RRR), autodiploid (RR), and haploid (R) gametes. On the basis of genetic composition of gamete, we speculate that some germ cells may perform the chromosome doubling by premeiotic endoreduplication, endomitosis, or fusion of oogonia germ in 4nRB ,, some of which show normal chromosome behavior (homologous chromosomes sets pair independently) during meiosis and developed into unreudced allotetraploid gametes, but other part of which show complete separation of the parental genomes, but not normal chromosome behavior during meiosis and develop into gametes with one or more RCC-derived chromosome sets. Of course, theoretically, other types of gametes with one or more sets of BSB-derived chromosomes may also have been produced because of complete separation of the parental genomes during meiosis, but were not detected in our study.
Diploid hybrid embryos (RB) of Carassius auratus red var. (2n = 100, RR, ♀) × Megalobrama amblycephala (2n = 48, BB, ♂) developed into surviving allotetraploid offspring (4nRB, RRBB) by somatic chromosome doubling ,. However, abnormal chromosome behavior during meiosis occurred in the allotetraploid fish to form gametes with different genetic compositions. This paper is the first detailed reports of abnormal chromosome behavior during meiosis in allotetraploid fish. Importantly, 4nRB is a significant experimental material for study of vertebrate chromosome evolution, and can provide an abundant gamete source for the production of other diploids or polyploids fish.
This research was supported by the National Natural Science Foundation of China (Grant No.31201987), the Major International Cooperation Projects of the National Natural Science Foundation of China (Grant No. 31210103918), the Doctoral Fund of Ministry of Education of China (Grant No.: 20124306120006), the Natural Science Foundation of Hunan Province (Grant No. 14JJ6008), the Educational Commission of Hunan Province (Grant No. 12B084), the Training Program of the Major Research Plan of the National Natural Science Foundation of China (Grant No. 91331105), the National Key Basic Research Program of China (Grant No. 2012CB722305), the National High Technology Research and Development Program of China (Grant No.2011AA100403), the Cooperative Innovation Center of Engineering and New Products for Developmental Biology, and the Construct Program of the Key Discipline in Hunan province and China.
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