Endless Forms Most Beautiful examines one of the most exciting aspects of evo devo--the incorporation of molecular biology that followed the discovery of classes of conserved regulatory (developmental, or "switching") genes: the homeobox, or Hox, genes. Carroll, who is a professor of genetics at the University of Wisconsin–Madison, writes in a lively style, peppering the book with endlessly fascinating examples that are beautifully illustrated by color and black-and-white drawings and photographs. To appreciate where this latest book devoted to evo devo is situated in the long history of the discipline, we need to go back almost 200 years.
The study of embryonic stages across the animal kingdom--comparative embryology--flourished from 1830 on. Consequently, when On the Origin of Species appeared in 1859, Charles Darwin knew that the embryos of all invertebrates (worms, sea urchins, lobsters) and vertebrates (fish, serpents, birds, mammals) share embryonic stages so similar (which is to say, so conserved throughout evolution) that the same names can be given to equivalent stages in different organisms. Darwin also knew that early embryonic development is based on similar layers of cells and similar patterns of cell movement that generate the forms of embryos and of their organ systems. He embraced this community of embryonic development. Indeed, it could be argued that evo devo (then known as evolutionary embryology) was born when Darwin concluded that the study of embryos would provide the best evidence for evolution.
Darwin's perception was given a theoretical basis and evo devo its first theory when Ernst Haeckel proposed that because ontogeny (development) recapitulates phylogeny (evolutionary history), evolution could be studied in embryos. Technological advances in histological sectioning and staining made simultaneously in the 1860s and 1870s enabled biologists to compare the embryos of different organisms. Though false in its strictest form, Haeckel's theory lured most morphologists into abandoning the study of adult organisms in favor of embryos--literally to seek evolution in embryos. History does repeat itself; 100 years later a theory of how the body plan of a fruit fly is established, coupled with technological advances, ushered in the molecular phase of evo devo evaluated by Carroll.
As Carroll discusses in his book (the title of which comes from the last lines of The Origin of Species), the discovery of Mendelian genetics in 1900, and soon after of the gene as the unit of heredity, thrust a wedge between development and evolution. Genes were now what mattered in evolution; embryos were merely the vehicles that carried genes from one generation to the next. Embryology was divorced from evolution, devo from evo. Even the discovery in the 1950s of the nature and role of DNA did not bring them back together. In the late 1970s, however, all began to change as several revolutions in theory and technology produced a mind shift as dramatic as the one that followed Darwin's The Origin of Species.
New methods for generating phylogenetic relationships brought comparative embryology back to the forefront; now we can assess the direction of evolutionary changes in development. When we find a species of frog that has lost the tadpole stage from its life cycle--a remarkable evolutionary change in form and function--we can determine whether that loss was an early or late event in the evolution of frogs. Stephen Jay Gould's seminal book Ontogeny and Phylogeny (1977) rekindled interest in 19th-century evolutionary embryology and resurrected an old idea--heterochrony, change in the timing of development in a descendant relative to an ancestor--in a form that could be tested. Important as these developments were, they were carried out against the then current wisdom that organisms differ because they possess unique genes not found in other organisms--lobster genes for lobsters, human genes for humans, and so forth.
The discovery of homeobox genes turned this approach upside down and inside out. The body plans of lobsters and humans, flies and fish, barnacles and mice, are initiated using the same families of genes that are conserved across the animal kingdom. The consequences of this discovery are the stuff of the first half of Endless Forms Most Beautiful, in which Carroll presents homeobox genes as the switches that contain the fundamental information required to make a fly's eye or a human hand.
The second half of the book explores what Carroll calls "the making of animal diversity," beginning with animal life as exemplified in the justly famous 500-million-year-old fossils of the Burgess Shale formation in British Columbia. Carroll is concerned with evolutionary tinkering with genetic switches and the production of patterns in nature--spots on butterfly wings, stripes on zebras. He devotes less attention to the downstream gene cascades and gene networks that allow similar signaling genes to initiate, for example, the wing of a bird or a human arm. Nor are the cells and cellular processes from which the endless forms are constructed given prominence.
Consequently, statements such as "the anatomy of animal bodies is really encoded and built ... by constellations of switches distributed all over the genome" could be taken to mean that switching genes contain all the information required to generate form. Were that true there would be no need for evo devo; indeed, there would be no development. It would all be geno evo. But, as Carroll demonstrates, "the evolution of form occurs through changes in development," which is precisely why evo devo is so central to understanding how animals have been and are being evolved.