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Chromosomal mapping of rDNAs and H3 histone sequences in the grasshopper rhammatocerus brasiliensis (acrididae, gomphocerinae): extensive chromosomal dispersion and co-localization of 5S rDNA/H3 histone clusters in the A complement and B chromosome

Nathalia L Oliveira1, Diogo C Cabral-de-Mello2, Marília F Rocha1, Vilma Loreto3, Cesar Martins4 and Rita C Moura1*

Author Affiliations

1 Departamento de Biologia, Instituto de Ciências Biológicas, UPE - Universidade de Pernambuco, Recife, Pernambuco, Brazil

2 Departamento de Biologia, Instituto de Biociências, UNESP - Universidade Estadual Paulista, Rio Claro, São Paulo, Brazil

3 Departamento de Genética, Centro de Ciências Biológicas, UFPE - Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil

4 Departamento de Morfologia, Instituto de Biociências, UNESP - Universidade Estadual Paulista, Botucatu, São Paulo, Brazil

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Molecular Cytogenetics 2011, 4:24  doi:10.1186/1755-8166-4-24

The electronic version of this article is the complete one and can be found online at: http://www.molecularcytogenetics.org/content/4/1/24


Received:2 September 2011
Accepted:10 November 2011
Published:10 November 2011

© 2011 Oliveira et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Supernumerary B chromosomes occur in addition to standard karyotype and have been described in about 15% of eukaryotes, being the repetitive DNAs the major component of these chromosomes, including in some cases the presence of multigene families. To advance in the understanding of chromosomal organization of multigene families and B chromosome structure and evolution, the distribution of rRNA and H3 histone genes were analyzed in the standard karyotype and B chromosome of three populations of the grasshopper Rhammatocerus brasiliensis.

Results

The location of major rDNA was coincident with the previous analysis for this species. On the other hand, the 5S rDNA mapped in almost all chromosomes of the standard complement (except in the pair 11) and in the B chromosome, showing a distinct result from other populations previously analyzed. Besides the spreading of 5S rDNA in the genome of R. brasiliensis it was also observed multiple sites for H3 histone genes, being located in the same chromosomal regions of 5S rDNAs, including the presence of the H3 gene in the B chromosome.

Conclusions

Due to the intense spreading of 5S rRNA and H3 histone genes in the genome of R. brasiliensis, their chromosomal distribution was not informative in the clarification of the origin of B elements. Our results indicate a linked organization for the 5S rRNA and H3 histone multigene families investigated in R. brasiliensis, reinforcing previous data concerning the association of both genes in some insect groups. The present findings contribute to understanding the organization/evolution of multigene families in the insect genomes.

Keywords:
evolution; genome; cytogenetics; multigene family

Background

In eukaryotes the transcribing sequences for ribosomal RNAs (rRNAs) are organized in two multigenic families tandemly arrayed in the genomes. The major one (45S rDNA) transcribes the 18S, 5.8S and 28S rRNAs and the minor one (5S rDNA) is responsible for the transcription of the 5S rRNA [1]. Concerning the histone gene sequences, they may be arranged in tandemly repeated clusters composed by intronless genes that codes for H1, H2A, H2B, H3 and H4 histone proteins spaced by noncoding DNA, although some variation has been reported for this organization [2,3].

Due to the clustered organization of multigene families and other repetitive DNAs they have been an important source as chromosomal marker for analysis of karyotypic evolution, genomic structure and origin and evolution of B chromosomes in animals. In grasshoppers the mapping of repeated elements is primarily concentrated in analysis of number and location of rDNAs and histone genes, and in the lesser extend satellite DNA (satDNAs) [4-9]. Concerning multigene families in Acrididae the major rDNA was mapped in 53 species, the histone genes were located in chromosomes of 39 species and the 5S rDNA distribution was described in about 30 species [4-7,9,10]. The mapping of these sequences together with the satDNA has been an important tool for understanding several aspects of the chromosome biology of acridid grasshopers [4,9,10].

Supernumerary B chromosomes occur in addition to standard karyotype and have been described in about 15% of eukaryotes. Some studies have been conducted on B elements, concerning their distribution, frequency in populations, structure and origin, effects in standard complement and transmission [11,12]. The B chromosomes are relatively well studied in grasshoppers, as for example in Eyprepocnemis plorans and Locusta migratoria. In this group variability for B chromosomes related to heterochromatin patterns, satellite DNAs organization and multigene families has been reported [4,9,10,12-14].

To advance in the understanding of chromosomal organization of multigene families (rDNAs and histone genes) among grasshoppers related to A complement and B chromosomes, we investigated here three populations of the species Rhammatocerus brasiliensis (Acrididae, Gomphocerinae) that presents a karyotype composed of 2n = 23, X0, acrocentric chromosomes in males, and bears a distinct B chromosome [10].

Methods

A total of 284 adult males of R. brasiliensis were collected in three distinct populations, Serra Talhada (07°59' 31'' S 38°17' 54'' W), 80 individuals; Surubim (07°49' 59'' S 35°45' 17'' W), 147 individuals; and from Vitória de Santo Antão (08°07' 05'' S 35°17' 29'' W), 57 individuals, Pernambuco State, Brazil. The animals were collected in the wild according to Brazilian laws for environmental protection (wild collection permit, MMA/IBAMA/SISBIO n. 2376-1). The experimental research on animals was conducted according to the international guidelines followed by São Paulo State University (Protocol no. 35/08 - CEEAA/IBB/UNESP). All animals were studied under conventional staining to estimate the B chromosome presence and frequency. For molecular cytogenetic analysis DNA and chromosomal spreads were obtained from ten individuals collected in Serra Talhada, six from Surubim and four from Vitória de Santo Antão. The genomic DNA of individuals without B chromosomes was extracted using the phenol-chloroform procedure described by Sambrook and Russel [15]. Meiotic chromosomes were obtained from testicular cells previously fixed in Carnoy (3:1 ethanol: acetic acid) and stored in freezer. The slides were prepared by classic squashing of testicular follicles technique using a drop of acetic acid (50%). Slides used for fluorescence in situ hybridization (FISH) analysis were prepared in 45% acetic acid and coverslips were removed after freezing the preparations by immersing in liquid nitrogen for a few seconds.

Partial sequences of 5S rRNA and histone H3 genes were amplified by PCR of genomic DNA from R. brasiliensis using the primers designated by Loreto et al. [10] and Cabral-de-Mello et al. [16], Sca5SF (5'-AAC GAC CAT ACC ACG CTG AA-3'), Sca5SR (5'-AAG CGG TCC CCC ATC TAA GT-3'), ScaH3F (5'-GGC NMG NAC NAA RCA RAC-3') and ScaH3R (5'-TGD ATR TCY TTN GGC ATD AT-3'). The 18S rDNA sequence was obtained from a cloned fragment previously isolated from the genome of Dichotomius semisquamosus [16].

The plasmid containing the 18S rRNA gene and the PCR product from histone H3 gene were labeled by nick translation using biotin-14-dATP (Invitrogen, San Diego, CA, USA). For simultaneous hybridization the 5S rDNA was labeled using digoxigenin-11-dUTP (Roche, Mannheim, Germany). The FISH procedures were performed according to the modifications of Cabral-de-Mello et al. [16]. The preparations were counterstained using the 4', 6-diamidine-2'-phenylindole dihydrochloride (DAPI) and mounted in Vectashield (Vector, Burlingame, CA, USA). Images were captured with the Olympus DP71 digital camera coupled to a BX61 Olympus microscope and were optimized for brightness and contrast using Adobe Photoshop CS2. The chromosomal morphology was defined using the description by Levan et al. [17].

Results

All populations of R. brasiliensis showed 2n = 23, X0 with acrocentric chromosomes (males), organized into three size-groups: three large (L1-L3), five medium (M4-M8) and three small (S9-S11). The X chromosome was identified as medium element and the B chromosome, when present, showed similar size to the X, as described by Loreto et al. [10,18]. A total of 26 individuals with B chromosome was observed in the total sample, being six from Serra Talhada, 11 from Surubim and nine from Vitória de Santo Antão, corresponding to 7, 5%, 7, 48% and 15, 79% of each sample, respectively [Loreto et al. in preparation].

The in situ hybridization of the 18S rDNA probe revealed that this sequence was located in the pericentromeric region of three autosomal chromosomes (M4, M6 and S9) in all populations analyzed (Figure 1a). The 5S rDNA was located in the pericentromeric region of all chromosomes of complement, including the X, except in the smallest autosome (S11) (Figure 1b). The dual-FISH indicated co-localization of 5S and 18S rRNA genes in the pairs M4, M6 and S9 (Figure 1a, b).

thumbnailFigure 1. Fluorescence in situ hybridization of 18S rRNA, 5S rRNA and H3 histone gene sequences in Rammathocerus brasiliensis without B and with 1B chromosome. (a-f) Metaphases I, (g) late diplotene and (h) diacinesis; (a) 18S rDNA; (b, e, g) 5S rDNA; (c, f, h) H3 histone; (d) DAPI only. In (c) is showed the H3 histone location in one individual from Surubim population and in the inserts in (h) are shown the hybridization patterns of 5S rDNA (red signals) and H3 (green signals) in the X and B chromosomes by two color FISH obtained from a Metaphase I. The smallest chromosome S11 that does not harbor 5S/H3 sites is indicated in (a, b, d, e, f). The X and B chromosomes, and chromosomes bearing specific hybridization (for 18S rDNA and H3 histone) signals are also indicated. Note the dispersion and co-localization of 5S rDNA and H3 histone sites, and the co-localization of 18S and 5S rDNA in three chromosomes. The meiotic plates in (g, h) are incomplete, lacking autosomes, but the X and B chromosomes are easily recognizable by their condensation patterns and univalent behavior. Chromosomes are counterstained with DAPI and the group of images (a, b) and (d, e, f) are the same metaphases submitted to two color FISH. Each bar = 5 μm.

The H3 histone gene was only observed in the pair M7 in one individual from Surubim (Figure 1c), while for the other individuals from this population and for the other two populations studied this gene family presented clusters in all chromosomes, except the S11. Two color FISH using 5S rRNA and H3 histone genes as probes confirmed the patterns obtained by single hybridization revealing loci dispersion for these sequences, being co-located in almost all chromosomes, except in the pair S11, that did not presented signals for the two genes (Figure 1e, f). The FISH for 5S rRNA and H3 histone genes in individuals with 1B revealed the presence of these genes in the B chromosome (Figure 1g, h). The double-FISH (5S rDNA and H3 histone gene) was performed, revealing co-localization for these genes in the centromeric region of the B element (Figure 1h-inserts).

Discussion

Standard chromosomal complement

The number of sites for 18S rDNA observed in the three populations of R. brasiliensis is coincident with the results published by Loreto et al. [10,18] for this species. The chromosomal mapping of 45S rDNA in grasshoppers has revealed an intense variability related to number and chromosomal location of this gene cluster. According to Cabrero and Camacho [6] the variability of rDNA in grasshoppers is caused probably by three mechanisms, structural chromosome rearrangements, ectopic recombination and transpositions. Similar mechanisms were also proposed for the 45 rDNA dispersion in other insects, as Scarabaeinae beetles and Lepidoptera representatives [19,20]. For R. brasiliensis the most plausible explanation is the transposition or occurrence of ectopic-recombination of major rDNA sites, since this species maintains the ancestral diploid number for Acrididae, and no evident macro-chromosomal rearrangement was observed in its karyotype. On the other hand, for other Gomphocerinae the action of large chromosomal rearrangements were important in changing of rDNA location, as described for species with 2n = 17,X0 [6].

The mapping of 5S rDNA in grasshoppers was performed in about 34 species, including four Proscopiidae and some Acrididae, being the number and chromosomal location conserved in the former and variable in the later [4,5,8-10]. In R. brasiliensis besides the spreading of major rDNA sites it was also observed a more intense dispersion for the 5S rDNA, for almost all chromosomes of the complement. High variability for 5S rDNA cluster number was also recently observed for other Acrididae species [5]. In this work the number of 5S rDNA sites observed in this species for all populations was distinct of the data previously described by Loreto et al. [10] that described 5S rDNA sites in the bivalents L3, M5, S11 and in the B chromosome. Our result points to a divergent condition of 5S rDNA organization and dispersion among the distinct populations of this species. The differential spreading for this sequence could be explained by differences in appropriate molecular mechanisms for 5S rDNA dispersion in the distinct populations, as proposed for major rDNA in grasshoppers as a whole [6]. The ability of major rDNA clusters to move and vary in number was first observed in Allium [21], and recently some additional evidence has accumulated concerning the ability of rDNA to move within the genome. Some studies have proposed that transposable elements are a potential source for the movement of rDNAs [22-24].

FISH using H3 histone sequence as probe also revealed dispersion for this gene sequence, being the pattern coincident to the same location of 5S rDNA, confirmed by two color FISH. In 35 species of Acrididae and four species belonging to Proscopiidae grasshoppers the number and location of histone genes were extremely conserved, with the presence of only one site [7,8]. Cabrero et al. [7] suggested that strong purifying selection could be operating in the non-spreading of histones in Acrididae grasshopper genomes, and Cabral-de-Mello et al. [8] by the analysis of four ancient grasshoppers (Proscopiidae) proposed that the genomic association of histones and 5S rRNA genes could be ancient for grasshoppers as a whole. Bearing in mind these hypotheses, it can be proposed a posterior dispersion of H3 gene in R. brasiliensis, being the ancestral characteristic the occurrence of only one site that occasionally was observed in the population sampled from Surubim. The spreading of H3 histone can be directly associated to the dispersion of 5S rDNA, indicating a linked organization of these two multigene families in the genome of R. brasiliensis, which causes the same evolutionary patterns for the two sequences. On the contrary, the analysis of other 29 Acrididae species revealed a distinct scenario, mainly without association of 5S rDNA/H3 histone sequences, being these elements co-located only in five species, but with non co-dispersion in species with 5S rDNA spreading (see Table 1). The linked organization of 5S rRNA and histone genes was observed for other invertebrate species, by molecular approach in one mussel [25] and two crustaceans [26,27]. Moreover by chromosomal analysis Cabral-de-Mello et al. [8,16,19] have proposed the association of these sequences in the genomes of insect representatives, such as in beetles and in four ancient grasshoppers (Proscopiidae), including the observation of co-dispersion. Further molecular analysis needs to be performed in R. brasiliensis and in other insects to confirm the genomic nature of the association of 5S rRNA and histone H3 genes.

Table 1. Grasshopper species with chromosomal co-localization of 5S rRNA and H3 histone genes.

Besides the co-localization of 5S rDNA and H3 histone sequences it was also observed a similar pattern for 18S and 5S rDNA in the chromosomal pairs M4, M6 and S9 of all populations. Loreto et al. [10] described these two ribosomal genes located in distinct chromosomes of R. brasiliensis, being identical the position of 18S rDNA observed here. Considering that the location of 18S rDNA is stable among the populations of R. brasiliensis, the co-location of ribosomal elements in the three studied populations might be explained by invasion of 18S rDNA or a near region by the 5S rRNA genes through transposition events. The movement of 5S rDNA through transposition has been documented for example in mammals [28] and fish [24]. Association/co-localization of 5S and major rRNA genes was also described in other invertebrates, such as annelids, mollusks and crustaceans and also in fungi [29-31]. On the other hand, in R. brasiliensis there is no evidence of interspersion of 18S rDNA and H3 histones genes, considering that the distribution in the histone gene clusters is not followed by dispersion of 18S genes.

The B chromosome

The B chromosome of R. brasiliensis is widely distributed among all population analyzed until the present time. Moreover a possible autosomal origin for this element using in situ hybridization for 5S and 45S rDNAs was proposed [10]. This conclusion was based on the presence of 5S rDNA sites restricted to autosomes and B element while absent in the X chromosome. On the contrary, our results cannot evidence an autosomal origin of the B chromosome in R. brasiliensis due the presence of 5S rDNA sites in almost all autosomes and also in the X chromosome, being this chromosomal marker non informative for B origin in this species. An alternative explanation can be the multiple origin of the B element in the distinct populations of R. brasisiensis studied with distinct conditions of 5S rDNA location. Multiregional origin for B chromosomes in grasshoppers was also previously proposed by Cabrero et al. [4] in E. plorans, using the mapping of rDNAs and a satellite DNA with 180 bp repeat sequences. Another limitation of the use of 5S rDNA sequence as an informative marker for definition of B origin and evolution is related to the intense evolutionary dynamics of this sequence in grasshopper genomes, as described by Cabral-de-Mello et al. [5]. In fact the presence of 5S rDNA in the B chromosome of R. brasiliensis could be a characteristic generated by transposition after the origin of this chromosome, and not a characteristic inherited from the chromosome responsible for its origin.

Besides the presence of 5S rDNA in B chromosomes of grasshoppers, satellite DNAs and 45S rDNA were also identified in this genomic element, as for example, in E. plorans and in some other animal groups, such as fish and mammals [4,32-34]. On the other hand, the presence of histone genes in B chromosomes was described only in one species until now, L. migratoria, being a good marker for discrimination of ancestry of this chromosome in this species [9]. The presence of H3 histone gene in the B chromosome of R. brasiliensis is the second case for grasshopper and for animal as a whole, indicating that in fact these chromosomes can harbor more gene sequences than was observed until now. Moreover, due the clustered organization of histone genes they can be a useful marker in the investigating of B origin. On the other hand, in the case of R. brasiliensis, this sequence, as well as the 5S rDNA, was not informative due their high dispersion. The presence of H3 gene in the B chromosome can be also directly associated with the dispersion of 5S rDNA, reinforcing the co-dispersion/co-localization of these two multigene families.

Conclusion

The results presented here reinforce the hypothesis of co-localization/association of the 5S rDNA and H3 histone genes in some insect groups, and other invertebrates. This association led to the same patterns of chromosomal dispersion of these two multigene families in the genome, including both A complement and B chromosomes. These results also contribute to a better knowledge about B chromosomes content in animal kingdom. Moreover, we bring attention in the definition of chromosomal markers to be applied for analysis of B origin, depending on the mechanisms of evolution for the chosen sequence in the genomes to be investigated. Specifically for the case of R. brasiliensis the ribosomal DNAs and histone genes apparently are not sufficient for definition of B origin, due their intense evolutionary dynamics leading to spread of clusters in the genome and remarkable differences among population of the species.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

NLO and DCCM carried out the conventional and molecular cytogenetic analysis and draft the manuscript. VL and MFR helped in the discussion of the obtained data. RCM, CM and DCCM conceived of the work, and participated in its design, drafted and revised the manuscript. All authors analyzed all results and read and approved the final manuscript. DCCM revised the manuscript with the suggestions from the reviewers.

Acknowledgements

The authors are grateful to Dr. N Santos for valuable suggestions and critical review of the manuscript, and to CA Ferreira and MP Santos (in memoriam) for assistance in the animal sampling in the field, and to the five anonymous reviewers for the suggestions. The study was supported by Coordenação de Aperfeiçoamento de Pesquisa de Nível Superior (CAPES) (scholarship to NLO and Grant number PROEQUIP 1752/2008 to CM), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (scholarship to DCCM), Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (FACEPE) (Grant number APQ-0583-2.02/06 to RCM), and Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP) (Grant number 2008/02832-4 to CM).

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