Hox genesis

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One of the hallmark characters of animals is the presence of a specific cluster of genes that are responsible for staking out the spatial domains of the body plan along the longitudinal axis. These are the Hox genes; they are recognizable by virtue of the presence of a 60 amino acid long DNA binding region called the homeodomain, by similarities in sequence, by their role as regulatory genes expressed early in development, by the restriction of their expression to bands of tissue, by their clustering in the genome to a single location, and by the remarkable collinearity of their organization on the chromosome to their pattern of expression: the order of the gene’s position in the cluster is related to their region of expression along the length of the animal. That order has been retained in most animals (there are interesting exceptions), and has been conserved for about a billion years.

Think about that. While gene sequences have steadily changed, while chromosomes have been fractured and fused repeatedly, while differences accumulated to create forms as different as people and fruit flies and squid and sea urchins, while continents have ping-ponged about the globe and meteors have smashed into the earth and glaciers have advanced and retreated, these properties of this set of genes have remained constant. They are fundamental and crucial to basic elements of our body plan, so basic that we take them completely for granted. They determine that we can have different regions of our bodies with different organs and organization. Where did they come from and what forces constrain them to maintain their specific organization on the chromosome? Are there other genes that are comparably central to our organization?

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Bilateral symmetry in a sea anemone

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There are quite a few genes that are known to be highly conserved in both sequence and function in animals. Among these are the various Hox genes, which are expressed in an ordered pattern along the length of the organism and which define positional information along the anterior-posterior axis; and another is decapentaplegic (dpp) which is one of several conserved genes that define the dorsal-ventral axis. Together, these sets of genes establish the front-back and top-bottom axes of the animal, which in turn establishes bilaterality—this specifically laid out three-dimensional organization is a hallmark of the lineage Bilateria, to which we and 99% of all the other modern animal species belong.

There are some animals that don’t belong to the Bilateria, though: members of the phylum Cnidaria, the jellyfish, hydra, sea anemones, and corals, which are typically radially symmetric. A few cnidarian species exhibit bilateral symmetry, though, and Finnerty et al. (2004) ask a simple question: have those few species secondarily reinvented a mechanism for generating bilateral symmetry (so that this would be an example of convergent evolution), or do they use homologous mechanisms, that is, the combination of Hox genes for A-P patterning and dpp for D-V patterning? The answer is that this is almost certainly an example of homology—the same genes are being used.

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Stromatoveris

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The Cambrian vendobiont S. psygmoglena, gen.sp.nov., composite photo of part and counterpart to show both upper and lower surfaces.

From the pre-Cambrian and early Cambrian, we have a collection of enigmatic fossils: the small shellies appear to be bits and pieces of partially shelled animals; there are trace fossils, the tracks of small, soft-bodied wormlike animals; and there are the very peculiar Edicaran vendobionts, which look like fronds and fans and pleated or quilted sheets. In the Cambrian, of course, we find somewhat more familiar creatures—sure, they’re weird and different, but we can at least tentatively see them as precursors to the modern members of their respective phyla. It’s not surprising, though, that the farther back in time we go, the stranger animals appear, and the more difficult it is to place them in our phylogenies.

So here’s something cool and helpful—it looks like a vendobiont, but it’s been found in the Lower Cambrian fossil beds of Chengjiang. It’s also very well preserved, and has features that suggest affinities to the ctenophores.

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Naked anaspids

This strange fish is Euphanerops longaevus, which is one of two species of 370 million year old jawless fishes (the other is Endeiolepis aneri, and the paper suggests that they may actually represent differently preserved members of the same species). These are soft-bodied animals that are usually poorly preserved, and are of interest because they seem to have some properties in common with both the lampreys and the gnathostomes, or jawed fishes. Their exact position in the vertebrate family tree is problematic, and the experts go back and forth on it; sometimes they are grouped with the lampreys, sometimes as cousins more closely related to the gnathostomes.

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Euphanerops longaevus, preserved as an imprint. Scale bar, 10 mm.

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Almost that time of year

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Hey! Coturnix is horning in on my turf, with a link to fornicating devil beetles (these are not popular beasties in my neighborhood—we get swarms of them every summer, crawling through every crevice to invade our house.)

It’s cool to see, but I may have to send a few of the boys over to the quail-man’s house to teach him a lesson. Either that or reconcile myself to the fact that my niche faces growing competition.

Evolving spots, again and again

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a–c, The wing spots on male flies of the Drosophila genus. Drosophila tristis (a) and D. elegans (b) have wing spots that have arisen during convergent evolution. Drosophila gunungcola (c) instead evolved from a spotted ancestor. d, Males wave their wings to display the spots during elaborate courtship dances.

It’s all about style. When you’re out and about looking for mates, what tends to draw the eye first are general signals—health and vigor, symmetry, absence of blemishes or injuries, that sort of thing—but then we also look for that special something, that je ne sais quoi, that dash of character and fashionable uniqueness. In humans, we see the pursuit of that elusive element in shifting fashions: hairstyles, clothing, and makeup change season by season in our efforts to stand out and catch the eye in subtle ways that do not distract from the more important signals of beauty and health.

Flies do the same thing, exhibiting genetic traits that draw the attention of the opposite sex, and while nowhere near as flighty as the foibles of human fashion, they do exhibit considerable variability. Changes in body pigmentation, courtship rituals, and pheromones are all affected by sexual selection, but one odd feature in particular is the presence of spots on the wing. Flies flash and vibrate their wings at prospective mates, so the presence or absence of wing spots can be a distinctive species-specific element in their evolution. One curious thing is that wing spots seem to be easy to lose and gain in a fly lineage, and species independently generate very similar pigment spots. What is it about these patterns that makes them simultaneously labile and frequently re-expressed?

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