- Open Access
Whole-genome analysis of animal A- and B-type cyclins
© Nieduszynski et al., licensee BioMed Central Ltd 2002
- Received: 30 May 2002
- Accepted: 3 October 2002
- Published: 15 November 2002
Multiple A- and B-type cyclins have been identified in animals, but their study is complicated by varying degrees of functional redundancy. A non-essential phenotype may reflect redundancy with a known or as yet unknown gene. Complete sequencing of several animal genomes has allowed us to determine the size of the mitotic cyclin gene family and therefore to start to address this issue.
We analyzed the Caenorhabditis elegans, Drosophila melanogaster and Homo sapiens genomes to identify known and novel A- and B-type cyclin genes and distinguish them from related pseudogenes. We find only a single functional A-type cyclin gene in invertebrates but two in vertebrates. In addition to the single functional cyclin A gene, the C. elegans genome contains numerous cyclin A pseudogenes. In contrast, the number and relationship of B-type cyclins varies considerably between organisms but all contain at least one cyclin B1-like gene and a cyclin B3 gene.
There are three conserved families of mitotic cyclins in animals: A-, B3- and B-type. The precise number of genes within the A- and B-type families varies in different organisms, possibly as an adaptation to their distinct developmental strategies.
- Additional Data File
- Human Genome Sequence
- Cleavage Division
- Cyclin Gene
- Mitotic Cyclins
Progression through the eukaryotic cell cycle is controlled by the sequential activation and inactivation of cyclin-dependent kinases (CDKs). The kinase activity of CDKs is regulated by cyclin synthesis and destruction, phosphorylation of the kinase and cyclin, binding to inhibitory polypeptides and subcellular localization. In metazoa there are four cyclin types (A, B, D and E) known to regulate cell-cycle transitions. These four cyclins have multiple isotypes, the precise number varying between organisms. In mammals and amphibians, members of the A- and D-cyclin families have been shown to be expressed in distinct cell types. In contrast, B-type cyclins are ubiquitous, being co-expressed in most, if not all, proliferating cells.
Both A- and B-type cyclins have been shown to have an essential role in progression into, through and out of M-phase. In vertebrates, two A-type cyclins have been identified to date. Cyclin A1 is expressed during meiosis, in early cleaving embryos [1,2] and in some transformed cell lines . Cyclin A2 is present in all proliferating cells from the beginning of S-phase until mitosis, with the exception of cells undergoing the meiotic division in males . The reason for this restricted expression pattern is unclear but male mice lacking the cyclin A1 gene are sterile owing to an arrest in meiosis . However, female mice lacking the cyclin A1 are fertile, possibly as a result of rescue by cyclin A2 which is expressed during female meiosis . Deletion of murine cyclin A2 is lethal; embryos are able to undergo the cleavage divisions but die immediately after implantation and appear unable to undergo proliferative growth  Ablation of expression of cyclin A2 in cultured cells leads to an arrest in S-phase or at the end of G2 .
Cyclin B-dependent kinase activity is essential for entry into mitosis. The best characterized vertebrate B-type cyclins, B1 and B2, are co-expressed in the majority of dividing cells, but are differentially localized within the cell (reviewed in ). Gene-deletion experiments have shown that mice lacking the cyclin B1 gene die in utero whereas mice lacking the cyclin B2 gene develop normally and have no immediately apparent phenotype . This suggests that loss of cyclin B2 can be compensated for by another cyclin, probably cyclin B1. Cyclin B3 is less well characterized, with a mammalian homolog only recently recognized . In Drosophila, cyclin B3 is not required for mitosis .
Redundancy between members of each cyclin class is probably responsible for the non-essential phenotypes described above. This effect is best understood in budding yeast, Saccharomyces cerevisiae, which has six B-type cyclins that display functional redundancy, yet fulfill distinct roles . To be better able to interpret the phenotypes of A- and B-type cyclin mutants in animals and the degree of redundancy that has to be taken into consideration, we have carried out a comprehensive search to identify A- and B-type cyclin genes in the completed Caenorhabditis elegans, Drosophila melanogaster and Homo sapiens genomes. The search has identified two novel B-type cyclin genes in C. elegans and has shown that there is only a single functional A-type cyclin gene in both invertebrates.
C. elegans: a single cyclin A gene and multiple cyclin A pseudogenes
The pseudogenes are found on all six chromosomes, and none is present in a tandem array. This contrasts with the arrangement of the major sperm protein (MSP), another C. elegans gene found in multiple copies. These genes (both transcribed and pseudogenes) are found in loose clusters of between 3 and 13 copies .
The cyclin A pseudogenes contain regions of sequence identity to each other which lie outside the region of identity to the cyclin A gene. These regions of identity extend over approximately 4.5 kilobase pairs (kbp) in total, and include direct and inverted repeats, some of which occur at other locations in the genome. This observation supports the possibility that the pseudogenes had a single origin and it is possible that the repeats have had a role in the transposition of the cyclin A pseudogenes around the genome.
C. elegans: multiple B-type cyclins
D. melanogaster: A- and B-type cyclins
The D. melanogaster genome sequence  was queried with the complete cyclin A protein sequence . Equivalent searches were performed using D. melanogaster cyclin B  and cyclin B3  protein sequences. Using all search permutations, only the three query sequences were identified. Therefore, it is highly probable that there is one A-type cyclin gene, a single cyclin B and a single cyclin B3 gene within the available sequence. No pseudogenes derived from any of these three cyclin genes were identified.
H. sapiens: A-type cyclins
The available human genome sequence (version 5.28.1)  was searched with cyclin A1 and A2 query sequences. In both cases the most significant matches were the two known A-type cyclins and the next most significant were the known B-type cyclins. Thus, there are only two A-type cyclin genes in the available sequence. No cyclin A-like pseudogenes were found.
H. sapiens: three B-type cyclins?
Searches of the available human genome sequence using B-type cyclin queries revealed three B-type cyclins - B1, B2 and B3 - but no other genes identifiable as encoding a functional B-type cyclin. Specifically, no homologs of the Xenopus cyclins B4 and B5  were found. Although the human genome sequence is not quite complete it seems unlikely that additional human B-type cyclins will be revealed.
Further evidence for this is provided by the lack of additional B-type cyclin sequences in the EST databases, in which cyclins B1, B2 and B3 were clearly present.
In addition to these three B-type cyclin genes, a region of high identity to cyclin B2 was found at chromosome 7p22.1. This region had the equivalent of 84% identity over 241 of the 398 amino acids of cyclin B2 and no identity outside this region. Thus the predicted open reading frame (ORF) contains only a fragment of the cyclin B2 gene and probably represents a pseudogene. There are no ESTs corresponding to this sequence in the database.
The main findings of this study are first, that invertebrates have a single A-type cyclin whereas vertebrates have two, and second, that the number of B-type cyclins varies from two in Drosophila to three in humans and four in C. elegans, but all have at least one cyclin B1-like gene and a cyclin B3 gene.
The intriguing question now is why vertebrates have evolved a distinct A-type cyclin with a limited role within the germline. One possible explanation is that cyclin A1 is part of the larger phenomenon of the occurrence of germline isoforms of a large number of genes. A number of enzymes are already known to have testis-specific isoforms (reviewed in ), including glyceraldehyde-3-phosphate dehydrogenase and phosphoglycerate kinase. In each case, testis-specific isoforms have been identified only in the vertebrate lineage (data not shown), suggesting that the second isoforms arose after the divide between invertebrates and vertebrates. It is clear that in invertebrates a single A-type cyclin can carry out all the functions of the mitotic and meiotic cell cycles.
Our finding of 15 cyclin A pseudogenes was unexpected, as the C. elegans genome is generally considered to contain a limited number of pseudogenes. However, the observation does explain the multiple restriction enzyme fragments that hybridize with a cyclin A probe on a Southern blot .
In each organism we identified a single B3-type cyclin, distantly related to both the A- and B-type cyclin families . The precise cellular role of cyclin B3 remains to be determined, although it appears to function late in mitosis . In Drosophila there is functional redundancy between the B and B3 cyclins in mitosis; however, deletion of both genes results in embryonic lethality. In contrast, both cyclins B and B3 are required for female fertility and cyclin B, but not B3, is required for male fertility. Therefore, it is possible that the mammalian B3 cyclins could also be partially functionally redundant with B-type cyclins.
The finding of three closely related C. elegans B-type cyclins has some significance in the interpretation of previously published data. RNA interference (RNAi) analysis of the nematode cyclin B resulted in embryonic lethality [24,25]. However, gene product ablation using RNAi may not distinguish between such high levels of identity and consequently the function of all three B-type cyclins will be lost, so the best interpretation possible is that at least one of these B-type cyclins is required. Additionally, three C. elegans cyclin B mRNAs of different lengths were observed and it was reported that they may arise from the use of different polyadenylation sites . An alternative interpretation, in the light of this study, is that each gene produces a single message so similar (approximately 80% nucleotide identity over the ORF) that the probes did not distinguish between them. Confirmation of this would require the generation of specific probes. One of the probes (a 3' UTR fragment) used by Kreutzer et al.  should have been specific for the previously identified cyclin B and did detect a single band. This allows us to predict that this gene gives rise to the largest (1.7 kbp) of the three transcripts. Interestingly, Kreutzer et al.  observed that the three cyclin B transcripts are differentially expressed in the maternal and paternal germlines. Therefore, it is possible that the three C. elegans cyclin B genes have distinct expression patterns through development.
The remaining vertebrate B-type cyclins fall into two evolutionarily divergent groups, one containing the B1 cyclins and the recently identified Xenopus cyclin B4 and the other the B2 cyclins and the Xenopus cyclin B5 . The genes encoding cyclins B1, B2 and B3 were readily identifiable within the draft human genome sequence; there are no other B-type cyclin genes present. Furthermore, homologs of the mitotic cyclins A1, A2, B1, B2 and B3 were readily identified in the extensive zebrafish EST database and the draft pufferfish genome database, but no cyclin B4 or B5 homologs were found. Together, this suggests that cyclins B4 and B5 are unique to amphibians, perhaps, as suggested by Hochegger et al. , as a requirement of their large eggs.
In conclusion we suggest that there are three conserved families of mitotic cyclins in animals: the A-type cyclins with one gene in invertebrates and two genes in vertebrates; the B3-type cyclins with a single gene in all animals; and the B-type cyclins with different numbers of genes in different organisms, possibly as an adaptation to their distinct developmental strategies.
BLAST 2.0 was used to carry out similarity searches against the available sequence databases with protein or DNA query sequences . For searches against the C. elegans and human genome sequences the Sanger Institute server  was used. For all other searches the NCBI server  was used.
The GCG Wisconsin Package Version 10.0 PileUp program was used for creating multiple sequence alignments (using progressive pairwise alignments); alignments were further refined using the CLUSTAL W program version 1.8  and manually. The TreeView program  was used for displaying and printing phylogenies produced by CLUSTAL W.
The alignments used for the construction of the phylogenetic trees of A- and B-type cyclins is available with the online version of this paper.
We thank Tim Hunt, Bill Colledge, Howard Baylis, Helena Webb and Catherine French for critical reading of the manuscript and/or helpful discussions. C.N. was the recipient of a BBSRC studentship.
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