At a scant 551 kilobases (kb), the nucleomorph genome of G. theta is one of the smallest and most gene-dense genomes known (1 gene per 977 base-pairs) [1]. Only the partially sequenced nucleomorph genome of an undescribed chlorarachniophyte species (CCMP621) is smaller, at 380 kb, and it is almost as gene-dense (1 gene per 1,141 base-pairs [9]). Studies in higher plants have shown that the vast majority of proteins required by the chloroplast are nucleus-encoded and are post-translationally targeted to the organelle after synthesis in the cytoplasm [10]. It follows, then, that the nucleomorph, once the nucleus of an alga, should be enriched for chloroplast genes. But sequencing of the G. theta nucleomorph has dispelled this assumption, because the genome encodes a mere 30 chloroplast proteins, even fewer than are in the chloroplast genome [1,11]. Most chloroplast genes appear to have been transferred to the nucleus of the host cell, and their proteins are targeted back to the chloroplast via the ER [12].

Most of G. theta's nucleomorph is occupied by a surprisingly diverse set of 'genetic housekeeping' genes [1]. These genes perform functions such as transcription, transcript processing (splicing, capping and polyadenylation), translation, protein folding and degradation, cell-cycle control, mitosis and some aspects of DNA packaging, synthesis and repair [1]. Some genetic housekeeping proteins expected to be present are in fact absent from the nucleomorph gene list, for example DNA polymerases and some ribosomal proteins. These are probably provided by the host cell, so although the endosymbiont is 'conceptually equivalent to a cell', it is not capable of living autonomously [1].

Of the 30 chloroplast proteins made by the nucleomorph, only two appear to be part of the photosynthetic apparatus [1]. Perhaps the tiny nucleomorph/periplastic compartment cannot synthesize chloroplast proteins in sufficient quantities to equip the organelle, or the photosynthetic genes are not tolerant of the elevated mutational environment in the nucleomorph. Preliminary data from the unfinished chlorarachniophyte nucleomorph genome indicate that it too encodes very few chloroplast genes [13]. Apart from chloroplast genes, very few other genes are present in the G. theta nucleomorph that encode functions directly useful to the rest of the cell [1]. These so-called 'end product' functions [14] include starch metabolism and ion transport as well as chloroplast functions [1].

In red algae starch is stored in the cytoplasm, and in the cryptomonad endosymbiont it is stored in an equivalent compartment, the periplastidal space (Figure 1). In chlorarachniophytes, carbohydrate storage has been transferred from the chloroplast to the host cell and changed from starch to a β1,3 glucan (Figure 1) [15]. It will be interesting to determine whether the transfer of carbohydrate metabolism from endosymbiont to host and the concomitant loss of genes for carbohydrate metabolism in chlorarachniophytes contributes to their nucleomorph genomes being smaller than those of cryptomonads. The function of nucleomorphs appears to be to produce a relatively small number of proteins vital for chloroplast and other cellular functions. But to produce these essential proteins nucleomorphs need a simplified gene-expression, DNA-replication and mitotic apparatus encoded by hundreds of additional genetic housekeeping genes.

Interestingly, the genomes of both cryptomonad and chlorarachniophyte nucleomorphs contain just three tiny chromosomes [13]. Douglas et al. [1] provide the first credible explanation for why both genomes, despite traveling independent evolutionary pathways, have arrived at similar endpoints. To start with, both genomes are similar in size because they contain a common core of genetic housekeeping genes. Some of these encode histones ([1] and my unpublished observations), so it is likely that the DNA is wound around histone cores. This would make the length of each chromosome about the width of a nucleomorph (1.5 μm), which means that each chromosome is just about the right size to be segregated by a mitotic spindle during mitosis. If there were fewer than three chromosomes they would be too long to be segregated within the confines of the nucleomorph, unless they were condensed into higher-order structures (which they appear not to be) [16]; if there were more than three chromosomes, each might be too small to be viable [17].

Nucleomorph chromosomes probably have centromeres, given that they encode centromere proteins [1]. It has been suggested that gene-free regions in the centres of each cryptomonad chromosome might comprise centromere DNA [1], although these regions lack any of the common repetitive motifs typical of centromeres [18]. In the G. theta nucleomorph all three tubulins (α, β and γ) are present, as well as centrosomal proteins, suggesting that the chromosomes may be segregated by a rudimentary spindle during mitosis [1,12].

The ends of nucleomorph chromosomes are also remarkably similar in both cryptomonads and chlorarachniophytes [5,19]. Each chromosome is capped with inverted repeats each comprising a single ribosomal DNA gene unit (rDNA; made up of 18S, 5.8S and 23S genes) linked to a telomere (Figure 1). The rDNA is in the opposite orientation relative to the telomeres in each type of nucleomorph. Presumably, recombination between chromosome ends and resultant gene convergence keeps the repeats of each chromosome identical to those of the other chromosomes [20]. Very few open reading frames reside in the inverted repeats, and it has been suggested that DNA replication origins may be located here as well [1].

Perhaps one of the most striking features of nucleomorphs is the extraordinary compactness of their coding sequences. Spacers between genes are extremely short, or in many cases entirely absent [1,19]. The coding sequences of some genes, encoded on opposite strands, overlap by as much as 76 base-pairs in the cryptomonad [1]. Such is the proximity of many genes that they must use cryptic regulatory sequences within the coding regions of neighboring genes. Chlorarachniophyte nucleomorph genes have a surfeit of pygmy-sized introns, ranging from 18 to 20 nucleotides in length, with 19 being the most common [19]. These introns still have standard GT-AG sequences at their borders, as do the introns in the cryptomonad nucleomorph. Cryptomonad introns, at 42-55 nucleotides, are somewhat larger than chlorarachniophyte introns, and the intron density is strikingly different between the two types of nucleomorph genome [1].

Chlorarachniophyte intron density, at 3.3 per kilobase of coding sequence, is only slightly less than average for eukaryotes (3.7 introns per kilobase) [21]. Genes of the cryptomonad nucleomorph, on the other hand, are intron-poor. The entire genome contains only 17 introns [22], which is fewer than the number of spliceosomal components required to remove them. The difference in intron density between the two types of nucleomorph probably reflects the intron density of their respective algal ancestors, indicating that once acquired introns are not easily lost, despite the efficacy with which other nucleomorph DNA has been removed during evolution [1,13].

Compared to the genomes of nucleomorphs, 91% of which are coding sequences [23], the genomes of most other eukaryotes, such as humans (1.5% coding sequence [24]), are positively flabby. The question of why eukaryotic genomes vary in size over many orders of magnitude (over 200,000-fold) is known as the C-value paradox (or C-enigma), and has not been settled yet (see [25] for recent discussion). One rule holds true, however: the genome size of an organism is proportional to its cell size, so big cells have big nuclei and hence big genomes. But this rule breaks down when applied to nucleomorphs. The genomes of these nuclei do not scale with cell size, although their host cell's nuclei do [14,23]. The factors that determine genome size in most cells have therefore apparently been suspended for nucleomorphs, and it has been proposed instead that there is strong selection for the removal of non-coding DNA [14,23]. Recently, however, it has been suggested (D. Petrov, personal communication) that a lack of transposable element activity may have reduced the amount of non-coding DNA in nucleomorphs, rather than there having been selection-driven DNA removal.

Transposable elements comprise 45% of the human genome, and much of the remaining non-coding DNA may be derived from the decaying sequences of ancient transposable elements [24]. Transposable elements have been discovered in nearly all eukaryotic species in which their presence has been assessed, and they are probably ubiquitous [26]. Interestingly, the only nuclei in which they have not been identified are nucleomorphs [19]. One possible explanation is that nucleomorphs are reproductively isolated from each other, because sexual stages between the host cells that would allow nucleomorphs/endosymbionts from different cells to occupy a common cytoplasm and to exchange DNA might be quite rare (and such sexual stages have yet to be well characterized) [27,28]. Even if host cell sex does occur, the extra membranes surrounding nucleomorphs are likely to form a barrier to DNA exchange. Transposable elements do not flourish in the absence of DNA exchange, and an entire class of transposable element that is present in sexual relatives is absent from asexual rotifers [26]. Without DNA exchange to introduce new transposable elements into nucleomorphs, the old ones will have been gradually inactivated by mutation. Without the DNA bulk-generating activity that results from transposable-element proliferation, small-scale deletions, which occur more frequently than insertions [22], will have removed all non-essential DNA sequences, including transposable elements, and nucleomorph genomes will therefore have become extremely compact. Another consequence of the absence of sexual DNA exchange is that those genes that do remain have often become highly divergent and are in some cases truncated [1].

It is probable that a lack of sex ultimately sealed the fate of nucleomorphs in the algae that have lost them. Nucleomorph genes encoding chloroplast or other end-product functions useful to the rest of the cell must have continuously accumulated errors that could not be corrected because recombination with fitter versions from other nucleomorphs was not possible. Nucleomorph genes may have eventually been replaced by fitter copies previously transferred to the host cell nucleus. These new proteins would have needed to acquire correct gene-regulatory information and protein-targeting addresses to be able to return to the endosymbiont from the host cell. It is possible that some nucleomorph genes were even replaced by duplicated versions of host-cell genes. Eventually, all essential end-product-function nucleomorph-encoded proteins were replaced by host-cell nuclear versions, until the nucleomorph's genetic housekeeping proteins had nothing left to make. Once this occurred, the nucleomorph would have rapidly been lost.

It is unknown whether a similar fate awaits cryptomonad and Chlorarachniophyte nucleomorphs or whether these genomes have now stabilized and will not lose many more genes, rather like the genomes of chloroplasts and mitochondria. Comparative analyses of chloroplast and mitochondrial genomes have revealed a core of genes commonly encoded by organelles and rarely encoded by nuclei. It is thought that because the concentrations of these proteins have to be continuously and rapidly adjusted they are made 'on site' and are therefore encoded by the organelle [29]. Comparative analysis of chlorarachniophyte and cryptomonad nucleomorph genome sequences may yet reveal a small core of genes with essential functions, which may be unwilling to take up residence in the host cell, so stalling the nucleomorph's demise. The insights gained from the sequence of G. theta's nucleomorph genome lead to great expectations of nucleomorph comparative genomics.