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Research Article

Cytogenetic Analyses Revealed Different Genome Rearrangement Footprints in Four ×Brassicoraphanus Lines with Different Fertility Rates

Hadassah Roa Belandres1, Hui Chao Zhou1, Nomar Espinosa Waminal1, Soo-Seong Lee2, Jin Hoe Huh3, Hyun Hee Kim1,*
Plant Breeding and Biotechnology 2019;7(2):95-105.
Published online: June 1, 2019

1Chromosome Research Institute, Department of Life Science, Sahmyook University, Seoul 01795, Korea

2BioBreeding Institute, Ansung 17544, Korea

3Department of Plant Science, Plant Genomics and Breeding Institute and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul 08826, Korea

*Hyun Hee Kim, kimhh@syu.ac.kr, Tel: +82-2-3399-1715, Fax: +82-2-3399-1729
• Received: March 14, 2019   • Revised: May 7, 2019   • Accepted: May 8, 2019

Copyright © 2019 The Korean Society of Breeding Science

This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • ×Brassicoraphanus (AARR, 2n = 38) is a synthetic intergeneric allopolyploid between Brassica rapa L. ssp. pekinensis (AA, 2n = 20) and Raphanus sativus L. var. rafiphera (RR, 2n = 18). Abnormalities in meiosis are main causes for infertility, especially in recent intergeneric allopolyploids. Several ×Brassicoraphanus lines showing varied fertility rates were produced previously, but no cytogenetic data specifying the reasons for infertility have been reported. In this study, we performed cytogenetic analyses in BB4, BB6, BB12, and BB50 lines to evaluate their chromosomal composition and behavior during meiosis. The four lines had relatively small chromosomes, ranging in length from 1.82 to 5.72 μm. BB6, BB12, and BB50 have euploid chromosome number of 2n = 38, whereas BB4 is an aneuploid with 2n − 1 = 37. Fluorescent in situ hybridization karyotype analysis by using 5S/45S rDNA revealed 5/7, 6/7, 5/5 and 5/5 pairs in BB4, BB6, BB12 and BB50, respectively. Genomic in situ hybridization analysis on cells in prophase I revealed varying frequencies of tetravalent pairing and sticky, ring, rod, and laggard chromosomes across the lines, which were more abundant in BB4 and BB6. Unlike BB4 and BB6, both BB12 and BB50 are known to have relatively higher seed fertility and uniform plant morphology. The varied degrees of chromosomal pairing stability during meiosis could explain the different fertility rates among the four ×Brassicoraphanus lines in this study. These data might facilitate breeding programs of ×Brassicoraphanus and further cytogenomic analyses.
  • Key words: Intergeneric hybrid, ×Brassicoraphanus, Cytogenetic study
In recent years, breeding of Brassica and Raphanus species has received considerable attention (Namai et al. 1980; Prakash et al. 2009) because of their agricultural importance worldwide as major crops as fodders, edible vegetables, and functional compounds sources (Lee et al. 2017). Brassica rapa (Chinese cabbage, 2n = 20) and Raphanus sativus (big root radish, 2n = 18) produce economically important shoot and root parts, respectively, especially in eastern Asia, where they are the main ingredients of staple foods like kimchi (Kim et al. 2000). While either shoot or root are utilized in either B. rapa and R. sativus, breeding for a species with combined shoot and root features of both species would optimize utility of plant parts. Thus, previous breeding efforts have initiated this program (Lee et al. 2002).
Morphological and cytological methods have been used to select synthetic hybrid species between the two genomes of Brassica and Raphanus (Dolstra 1982; Kato and Tokumasu 1983). A newly synthesized intergeneric allotetraploid, ×Brassicoraphanus, was developed by crossing B. rapa L. ssp. pekinensis and R. sativus (Lee et al. 1999; Lee et al. 2002; Lee et al. 2017); however it was found to be unstable with low seed fertility and uniformity. The progenies from these unstable materials were stabilized using microspore mutagenesis by using N-nitroso-N-methyl urethane (NMU) (Lee et al. 2011; Lee et al. 2017). The same procedure involving the use of NMU was applied to develop another allotetraploid hybrid between B. rapa L. ssp. pekinensis and R. sativus L. var. rafiphera, and the F1 hybrid was crossed with a mutagen-induced stabilized line to produce different lines of ×Brassicoraphanus.
Before the development of fluorescence in situ hybridization (FISH), chromosome-based cytogenetic studies performed using conventional staining method were applied to Brassica species; however, the technique limited the evaluation among the homologous chromosomes with similar size (Olin-Fatih and Heneen 1992; Olin-Fatih 1994; Cheng et al. 1995; Hwang et al. 2009). Chromosome characterization and genome identification have been advanced significantly with the development of molecular cytogenetics involving the use of FISH and genomic in situ hybridization (GISH) techniques (Fukui 2005; Capdeville et al. 2008; Park et al. 2010; Hwang et al. 2012; Pendinen et al. 2012). These methods have been used to investigate allopolyploid species (Yang et al. 1999; Cao 2003; Devi et al. 2005), recombinant breeding lines (Lou et al. 2010; Vasconcelos et al. 2010; Hwang et al. 2012), and genome structure and inter-genomic relationships of hybrid plants (Kenton et al. 1993; Jellen et al. 1994).
Tandemly repeated short sequences or multigene families, including 5S and 45S ribosomal DNAs (rDNAs), have primarily been used as cytogenetic markers in FISH (Kato et al. 2004; Lim et al. 2005; Lim et al. 2012). Maluszynska and Heslop-Harrison (1993) first reported the number of 45S rDNA loci in diploids and allotetraploids of Brassica.
Recently, a FISH karyotype analysis of ×Brassicoraphanus line BB#5 (Belandres et al. 2015) and a conventional Giemsa-staining karyotype analysis of line BB4 were conducted (Lim et al. 2012), however no cytogenetic data on the developed hybrid lines is available. In this study, we analyzed the chromosomal distribution and localization of 5S and 45S rDNA on four synthetic hybrid lines and constructed a dual-color FISH karyotype with both markers to identify the chromosome complement of each inbred line. Moreover, meiotic chromosome pairing patterns were analyzed to discriminate both parental genomes, Brassica and Raphanus, by using GISH method.
Plant materials
The floral buds and seeds of the ×Brassicoraphanus lines BB4, BB6, BB12, and BB50 were kindly provided by Soo-Seong Lee who developed the intergeneric hybrids in the Bio-Breeding Institute, Ansung, Korea. The floral buds were collected from the adult plants of each line and the seeds were sent for this experiment after harvesting from each line. The seeds were germinated in Petri dishes with moist filter paper at 25°C for 48 hours. Root tips (length, 2 cm) were harvested and pretreated with 2 mM 8-hydroxyquinoline at 18°C for 5 hours, fixed in aceto-ethanol (1:3 v/v) solution for 2 to 24 hours, and then stored in 70% ethanol until use. Floral buds were fixed in the same solution for 24 hours and stored in 70% ethanol at −20°C.
Chromosome and probe preparation for FISH and GISH
Mitotic and meiotic chromosomes, rDNA probes, FISH and GISH procedures were done following the same procedures of previous study (Belandres et al. 2015).
Homologous chromosomes were identified based on the FISH karyotype of ×Brassicoraphanus line BB5 (Belandres et al. 2015). Meiotic pairing configurations were analyzed in late prophase I. The varying degree of meiotic abnormalities were examined in 500 pollen mother cells (PMCs).
rDNA repeats
The fluorescence in situ hybridization (FISH) karyotype of ×Brassicoraphanus lines with 5S/45S rDNA revealed 5/7, 6/7, 5/5, and 5/5 pairs in BB4, BB6, BB12, and BB50, respectively (Figs. 1 and 2, Table 1). The 5S rDNA loci were observed in the para-centromeric region of the long arms of chromosomes 2 and 7, terminal part of the short arms of chromosome 13 and 14 being juxtaposed to the satellite chromosome, and on the terminal part of the short arm of chromosome 16. However, in BB6, another pair of 5S rDNA loci was observed in the para-centromeric region of the long arm of chromosome 9. The 45S rDNA loci pattern of BB12 and BB50 was identical, whereas two more pairs were observed for BB4 and BB6 (Figs. 1 and 2, Table 1). The 45S rDNA loci were observed at the paracentromeric region of the long arms of chromosomes 4, 6, and 7 and on the nuclear organizer region (NOR) regions of chromosome 13 and 14. However, two additional pairs of 45S rDNA loci were observed in the para-centromeric region of the long arms of chromosome 5 and 9 in BB6 and the para-centromeric region of the long arms of chromosome 5 and near the short arm of chromosome 11 in BB4.
When compared with the FISH karyotype of the stable line BB5, some of the 45S rDNA loci were absent, particularly in chromosome 8 of BB4, chromosomes 8 and 11 of BB6, and chromosomes 5, 8, and 11 of BB12 and BB50. However, the five pairs of 5S rDNA loci were all present in the four lines. In addition, a distinct pair of co-localized 5S and 45S rDNA loci was observed only in chromosome 9 of BB6, which was even absent in BB5.
FISH karyotype
BB4 was aneuploidy with a somatic chromosome number of 2n − 1 = 37 (Fig. 1A, E), with lengths ranging from 1.82 to 3.45 μm and a total length of 49.64 μm (Table 1). The chromosome complement comprised fifteen metacentric and four submetacentric chromosomes. Chromosome 12 of BB4 has a missing copy of its homolog, resulting in a low total chromosome length compared to that for the other lines (Fig. 1E, white arrows). BB6 somatic chromosome number was 2n = 38 (Fig. 1B and F), with lengths ranging from 2.31 to 4.43 μm and a total length of 61.39 μm (Table 1). The chromosome complement comprised fifteen metacentric and four submetacentric chromosomes. BB12 somatic chromosome number was 2n = 38, (Fig. 1C and G), with chromosome lengths ranging from 2.58 to 4.78 μm and a total length of 68.02 μm (Table 1). The chromosome complement comprised eighteen metacentric and one submetacentric chromosomes. BB50 chromosome number was 2n = 38 (Fig. 1D and H), with lengths ranging from 2.40 to 5.72 μm and a total length of 74.34 μm (Table 1). The chromosome complement comprised twelve metacentric and seven submetacentric chromosomes (Fig. 2).
Meiotic chromosome behavior
GISH analysis was done to identify chromosomes from each parent, B. rapa (Fig. 3B–K, raw) and R. sativus (Fig. 3A–J, DAPI-blue) on the PMCs at prophase I of meiosis in the four lines (Fig. 3). In meiotic pairing, nineteen bivalent chromosome pairs were observed in BB50 (Fig. 3J–L), consisting of ten and nine bivalent chromosome pairs of B. rapa (Fig. 3J, red arrowheads, K-raw) and R. sativus, respectively (Fig. 3J, white arrowheads), whereas the rest of the lines BB4, BB6, and BB12 consisted of combined bivalent and tetravalent chromosome pairs from both the genomes (Fig. 3A–I). For instance, BB4 has six bivalent (Fig. 3A, red arrowheads) and two tetravalent chromosome pairs of B. rapa (Fig. 3A, red asterisk, B-raw), and seven bivalent (Fig. 3A, white arrowheads) and one tetravalent chromosome pairs from R. sativus (Fig. 3A, white asterisk); BB6 has nine bivalent (Fig. 3D, red arrowheads) and two univalent chromosome pairs of B. rapa (Fig. 3D, yellow arrowheads, E-raw) and five bivalent (Fig. 3D, white arrowheads) and two tetravalent chromosome pairs from R. sativus (Fig. 3D, white asterisk); BB12 has eight bivalent (Fig. 3G, red arrowheads) and one tetravalent chromosome pairs from B. rapa (Fig. 3G, red asterisk, H-raw) and nine bivalent chromosome pairs of R. sativus (Fig. 3G, white arrowheads).
Meiotic abnormalities were noted in all lines from different stages of meiosis, although all the lines were not equally affected. The irregularities observed include chromosome stickiness (Fig. 4A), rings (Fig. 4B, yellow arrowheads), rods (Fig. 4B, red arrowheads), laggard chromosomes (Fig. 4C–G, red arrowheads), and bridge fragmentation (Fig. 4E, yellow arrowheads). In addition, micronuclei (Fig. 4H, red arrowheads) were identified in telophase II due to acentric chromosome fragments or lagging chromosomes that were not incorporated into one of the daughter nuclei during cell division. The unstable lines BB4 and BB6 showed high frequencies of meiotic abnormalities, which accounted for 57% (287) and 34% (169), respectively, compared to 12% (60) and below in the stable lines BB50 and BB12. High degree of laggard chromosomes in metaphase I was observed, which accounted for 31% (154), followed by bridge fragmentation in anaphase I for 10% (49) in BB4, whereas laggards in metaphase I and II accounted for 13% (65) and 7% (36) in BB6, examined using 500 PMCs (Table 2).
Intergeneric allopolyploids between Brassica and Raphanus have remained unstable despite numerous attempts to improve their chromosomal pairing stability. However, Lee et al. (2011) successfully developed stable progenies, ×Brassicoraphanus, through induced mutation by using microspore culture, which became a commercial vegetable crop. In this study, we assessed the somatic metaphase chromosome karyotype by fluorescence in situ hybridization (FISH), meiotic pairing behavior by genomic in situ hybridization (GISH) and meiotic abnormalities in four lines of ×Brassicoraphanus.
Various studies have been conducted on cytogenetics of natural and synthetic allopolyploids (Bennett et al. 1992; Yao et al. 2010; Fujii and Ohmido 2011). FISH karyo-typing has been found to be a useful method for identification of each chromosome homolog and providing detailed chromosomal information of a genome. The two rDNA families, the non-NOR-forming 5S rDNA and NOR-forming 45S rDNA (Singh et al. 2009), which are composed of many repeat units, have been primarily used as FISH probes (Hasterok et al. 2006; Lim et al. 2007; Fujii and Ohmido 2011). These two rDNAs have been used in phylogenetic studies in which the varying distribution patterns among species and population have been exploited (Drouin and de Sá 1995). Reports on FISH karyotype by using 5S and 45S rDNA probes showed three 5S and five 45S rDNA pairs in Brassica rapa (Lim et al. 2005; Hwang et al. 2009; Koo et al. 2011; Xiong and Pires 2011; Belandres et al. 2015), whereas two 5S and three 45S rDNA pairs in Raphanus sativus (Hwang et al. 2012; Belandres et al. 2015). A recent study showed that both Brassica- and Raphanus genomes-derived 5S and 45S rDNA distribution patterns showing eight and five pairs of 5S and 45S rDNA loci, respectively, were identified in a stable allopolyploid hybrid ×Brassicoraphanus line, BB5 (Belandres et al. 2015).
In this study, we observed varying numbers of 5S and 45S rDNA loci within and among the several lines of ×Brassicoraphanus. However, two pairs of nucleolar organizers of Brassica and Raphanus were present in all lines. These factors might have contributed to the concerted changes in multiple tandem repeats (Eickbush and Eickbush 2007), in which the common mechanisms involve unequal crossing-over and gene conversion (Dover 1989; Shaked et al. 2001). In addition, these changes in rDNA distribution can be attributed to genomic rearrangements that include rDNA loci exchanges, fragment loss, and homoeologous exchange, as reported previously (Pontes et al. 2004; Gaeta et al. 2007; Lim et al. 2008). Major karyotypic changes such as aneuploidy can result in alterations and irregularities in somatic and meiotic cell division. Meiotic mechanisms inducing aneuploidy might include non-homologous recombination, asynapsis, loss of recombination and chromosome segregation defects in meiosis (Cai and Xu 2007; Ravi et al. 2011). In general, allopolyploids show genetic and phenotypic changes because of chromosomal rearrangement, gene dosage effects, unbalanced parental genome contributions, existence of different genomes in the nucleus, and variations in chromosome number (Leitch and Leitch 2008). In a synthetic hybrid, several chromosomal variations and abnormal meiosis were observed, implying that the genetic instability of the hybrid polyploid was due to abnormal chromosome number and structure, which were attributed to aberrant meiosis (Fujii and Ohmido 2011). In the present study, the unstable line BB4 was aneuploid with 2n −1 = 37, showing a high degree of meiotic irregularities and nondisjunction and anaphase chromosome lagging could be the two mechanisms responsible for chromosome loss or aneuploidy. The nuclear envelope was formed with a laggard might form a micronucleus.
Brassicaceae interspecific hybrid subgenomes were successfully identified using GISH method (Wang et al. 2006; Yao et al. 2010; Howell and Armstrong 2013). Moreover, the parental subgenomes, Brassica and Raphanus, were clearly discriminated in somatic metaphase (Lim et al. 2012) and meiotic chromosomes (Belandres et al. 2015) of the hybrid ×Brassicoraphanus. In this study, we discriminated ten and nine pairs of Brassica and Raphanus bivalent chromosomes in BB50, and the remaining lines BB4, BB6, and BB12 consisted of the combined univalent, bivalent, and tetravalent chromosome pairs of both parental sub-genomes. Genomic reports showed that a high degree of synteny is shared between B. rapa and R. sativus genomes (Kitashiba et al. 2014; Moghe and Shiu 2014). This might imply that multivalent chromosome pairing between B. rapa and R. sativus chromosomes might be attributed to the possible pairing of nonhomologous chromosomes to the homeologous region at the early stage of meiosis. In addition, multivalent formation can be generated because of chromosomal changes due to abnormal segregation in meiosis (Comai 2005; Leitch and Leitch 2008; Fujii and Ohmido 2011), which could increase the chance of chromosomal rearrangement such as translocation and deletion over two nonhomologous chromosomes during segment exchange, leading to genome instability and infertility of hybrid allopolyploid plants.
Different levels of meiotic irregularities are possible in allopolyploid because of segmental interchange during homeologous recombination influenced by the progenitor genotype and/or their combination (Szadkowski et al. 2010; Grandont et al. 2014). We observed several chromosomal abnormalities in different stages of meiosis. Chromosome stickiness is characterized by an intense clumping of chromosomes during any phase of the cell cycle (Rao et al. 1990; Kiihl et al. 2011). This might have been caused by environmental factors such as ionizing radiation, temperature, and soil elements (Mendes-Bonato et al. 2001). Ring chromosomes might form in cells following genetic damage by mutagens where both ends of the chromosome were often missed, enabling the broken ends to fuse together to form a ring. Laggard chromosomes may either be excluded or rejoined forming daughter nuclei later than the other chromosomes (De Storme and Mason 2014). This is common in hybrids and new allopolyploids might go through unequal interaction of centromeres and the loss of centromeric histone H3 (CenH3) (Ravi and Chan 2010), causing subsequent chromosome loss and uniparental genome elimination (Sanei et al. 2011). In some cases, incorrect chromosome segregation can lead to bridge and bridge fragmentations (Kiihl et al. 2011) and can be attributed to chromatin breakage and fusion or breakage due to the failure of chiasma termination that leads to subsequent lagging at anaphase I (Saylor and Smith 1966).
Advanced molecular cytogenetic studies including FISH and GISH using chromosome-specific DNA markers and comparative studies related to genome sequencing are necessary to elucidate more accurate genome structures of the hybrid lines. Our results might be useful for further genomic study of ×Brassicoraphanus lines and their improvement as new promising breeding varieties.
This work was supported by the Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (IPET) through the Agri- Bio Industry Technology Development Program, funded by the Ministry of Agriculture, Food and Rural Affairs (MAFRA; 117045-3).
Fig. 1
Dual color FISH metaphase of the four inbred lines of ×Brassicoraphanus. Three mitotic metaphase spreads of lines BB6 (B, F), BB12 (C, G), BB50 (D, H) showing chromosome number 2n = 38, and BB4 (A, E, arrow), 2n − 1 = 37. The 5S and 45S rDNA loci are shown as green and red signals, respectively. FISH metaphase chromosomes were arranged in decreasing order according to the length and morphology of each chromosome (E–H). Line BB4 has an incomplete chromosome number indicated by an arrow (E). Scale bar, 5 μm.
pbb-7-095f1.jpg
Fig. 2
FISH karyotypic idiograms showing chromosome number, length, morphology, and 5s and 45s rDNAs signals in ×Brassicoraphanus inbred lines, BB4 (2n − 1 = 37, A) with missing chromosomes indicated by an arrow, BB6 (2n = 38, B), BB12 (2n = 38, C), and BB50 (2n = 38, D). The 5S and 45S rDNA loci are shown as green and red signals, respectively. The chromosomes were arranged according to the length, morphology, and rDNAs distribution described by Belandres et al. (2015).
pbb-7-095f2.jpg
Fig. 3
Meiotic chromosome pairing in prophase I of ×Brassicoraphanus inbred lines BB4 (A–C), BB6 (D–F), BB12 (G–I), and BB50 (J–L). Nineteen complete bivalents were observed in BB50, as shown in (J), 10 of which are of B. rapa (green fluorescence, K- raw) and nine are of R. sativus chromosomes (DAPI, blue), whereas the remaining lines show multivalent and univalent chromosome pairing. In the panels above, white arrowheads and white asterisks indicate R. sativus chromosomes; red arrowheads, red asterisks, and the raw images in the middle panels are of B. rapa; yellow arrowheads indicate univalent chromosomes; and asterisks (red and white) indicate tetravalent chromosomes. The bottom panels are raw DAPI images of the four lines. Scale bar, 5 μm.
pbb-7-095f3.jpg
Fig. 4
Meiotic abnormalities observed in the four lines of ×Brassicoraphanus. (A–H) DAPI raw images of abnormal cells observed including sticky chromosomes (A), ring (yellow arrows) and rod (red arrows) (B), lagging chromosomes in metaphase I/II and anaphase I/II (C–G, red arrows), bridge fragmentation in anaphase I and telophase II (E, H, yellow arrows) with two micronuclei (H, red arrow), all of which contributes to the characteristic increase in aneuploidy and sterility.
pbb-7-095f4.jpg
Table 1
Summary of FISH karyotype analyses of intergeneric hybrid × Brassicoraphanus lines BB4, BB6, BB12, and BB50.
Table 1
Inbred lines Chr. no. (2n) Chr. length (μm) rDNA signals Karyotype formula (2n)
Shortest Longest Total 5S 45S
BB4 37 1.82 3.45 49.69 5 7 2m + 2m + 2sm + 2m + 2m + 2m + 2m + 2m + 2m + 2sm + 2m + 2m + 2smz) + 2mz) + 2m + 2sm + 2m + 2m + 2m
BB6 38 2.31 4.43 61.39 6 7 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2sm + 2sm + 2smz) + 2mz) + 2sm + 2m + 2m + 2m + 2m
BB12 38 2.58 4.78 68.02 5 5 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2smz) + 2mz) + 2m + 2m + 2m + 2m + 2m
BB50 38 2.40 5.72 74.34 5 5 2m + 2m + 2m + 2m + 2sm + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2smz) + 2mz) + 2sm + 2sm + 2sm + 2sm + 2sm

z)satellite chromosomes. m: metacentric, sm: submetacentric.

Table 2
The frequency of meiotic abnormalities in different meiotic stages of the four inbred lines of ×Brassicoraphanus.
Table 2
Stages No. of abnormal PMCs
BB4 BB6 BB12 BB50
Prophase I (diakinesis)
 Sticky chromosomes 35 28 4 6
 Rod/ring chromosomes 18 7 8 0
 Laggard chromosomes 22 5 12 5
Metaphase I
 Laggard chromosomes 154 65 15 17
Anaphase I
 Bridge fragmentation 49 14 5 27
Metaphase II
 Laggard chromosomes 8 36 6 5
Anaphase II
 Bridge fragmentation 1 9 0 0
Total meiotic abnormality (%)
 (per 500 PMCs)		 287 (57%) 169 (34%) 50 (10%) 60 (12%)
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Cytogenetic Analyses Revealed Different Genome Rearrangement Footprints in Four ×Brassicoraphanus Lines with Different Fertility Rates
Plant Breed. Biotech.. 2019;7(2):95-105.   Published online June 1, 2019
DOI: https://doi.org/10.9787/PBB.2019.7.2.95
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Cytogenetic Analyses Revealed Different Genome Rearrangement Footprints in Four ×Brassicoraphanus Lines with Different Fertility Rates
Plant Breed. Biotech.. 2019;7(2):95-105.   Published online June 1, 2019
DOI: https://doi.org/10.9787/PBB.2019.7.2.95
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Cytogenetic Analyses Revealed Different Genome Rearrangement Footprints in Four ×Brassicoraphanus Lines with Different Fertility Rates
Image Image Image Image
Fig. 1 Dual color FISH metaphase of the four inbred lines of ×Brassicoraphanus. Three mitotic metaphase spreads of lines BB6 (B, F), BB12 (C, G), BB50 (D, H) showing chromosome number 2n = 38, and BB4 (A, E, arrow), 2n − 1 = 37. The 5S and 45S rDNA loci are shown as green and red signals, respectively. FISH metaphase chromosomes were arranged in decreasing order according to the length and morphology of each chromosome (E–H). Line BB4 has an incomplete chromosome number indicated by an arrow (E). Scale bar, 5 μm.
Fig. 2 FISH karyotypic idiograms showing chromosome number, length, morphology, and 5s and 45s rDNAs signals in ×Brassicoraphanus inbred lines, BB4 (2n − 1 = 37, A) with missing chromosomes indicated by an arrow, BB6 (2n = 38, B), BB12 (2n = 38, C), and BB50 (2n = 38, D). The 5S and 45S rDNA loci are shown as green and red signals, respectively. The chromosomes were arranged according to the length, morphology, and rDNAs distribution described by Belandres et al. (2015).
Fig. 3 Meiotic chromosome pairing in prophase I of ×Brassicoraphanus inbred lines BB4 (A–C), BB6 (D–F), BB12 (G–I), and BB50 (J–L). Nineteen complete bivalents were observed in BB50, as shown in (J), 10 of which are of B. rapa (green fluorescence, K- raw) and nine are of R. sativus chromosomes (DAPI, blue), whereas the remaining lines show multivalent and univalent chromosome pairing. In the panels above, white arrowheads and white asterisks indicate R. sativus chromosomes; red arrowheads, red asterisks, and the raw images in the middle panels are of B. rapa; yellow arrowheads indicate univalent chromosomes; and asterisks (red and white) indicate tetravalent chromosomes. The bottom panels are raw DAPI images of the four lines. Scale bar, 5 μm.
Fig. 4 Meiotic abnormalities observed in the four lines of ×Brassicoraphanus. (A–H) DAPI raw images of abnormal cells observed including sticky chromosomes (A), ring (yellow arrows) and rod (red arrows) (B), lagging chromosomes in metaphase I/II and anaphase I/II (C–G, red arrows), bridge fragmentation in anaphase I and telophase II (E, H, yellow arrows) with two micronuclei (H, red arrow), all of which contributes to the characteristic increase in aneuploidy and sterility.

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Fig. 4

Cytogenetic Analyses Revealed Different Genome Rearrangement Footprints in Four ×Brassicoraphanus Lines with Different Fertility Rates

Summary of FISH karyotype analyses of intergeneric hybrid × Brassicoraphanus lines BB4, BB6, BB12, and BB50.

Inbred lines Chr. no. (2n) Chr. length (μm) rDNA signals Karyotype formula (2n)
Shortest Longest Total 5S 45S
BB4 37 1.82 3.45 49.69 5 7 2m + 2m + 2sm + 2m + 2m + 2m + 2m + 2m + 2m + 2sm + 2m + 2m + 2smz) + 2mz) + 2m + 2sm + 2m + 2m + 2m
BB6 38 2.31 4.43 61.39 6 7 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2sm + 2sm + 2smz) + 2mz) + 2sm + 2m + 2m + 2m + 2m
BB12 38 2.58 4.78 68.02 5 5 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2smz) + 2mz) + 2m + 2m + 2m + 2m + 2m
BB50 38 2.40 5.72 74.34 5 5 2m + 2m + 2m + 2m + 2sm + 2m + 2m + 2m + 2m + 2m + 2m + 2m + 2smz) + 2mz) + 2sm + 2sm + 2sm + 2sm + 2sm

z)satellite chromosomes. m: metacentric, sm: submetacentric.

The frequency of meiotic abnormalities in different meiotic stages of the four inbred lines of ×Brassicoraphanus.

Stages No. of abnormal PMCs
BB4 BB6 BB12 BB50
Prophase I (diakinesis)
 Sticky chromosomes 35 28 4 6
 Rod/ring chromosomes 18 7 8 0
 Laggard chromosomes 22 5 12 5
Metaphase I
 Laggard chromosomes 154 65 15 17
Anaphase I
 Bridge fragmentation 49 14 5 27
Metaphase II
 Laggard chromosomes 8 36 6 5
Anaphase II
 Bridge fragmentation 1 9 0 0
Total meiotic abnormality (%)
 (per 500 PMCs)		 287 (57%) 169 (34%) 50 (10%) 60 (12%)
Table 1 Summary of FISH karyotype analyses of intergeneric hybrid × Brassicoraphanus lines BB4, BB6, BB12, and BB50.

satellite chromosomes. m: metacentric, sm: submetacentric.

Table 2 The frequency of meiotic abnormalities in different meiotic stages of the four inbred lines of ×Brassicoraphanus.

Table 1

Table 2

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