Developmental Endocrinology of the Dipnoan, Neoceratodus forsteri

The development of the pineal, pituitary and thyroid glandsof the extant lungfish, Neoceratodus forsteri, are being studiedboth morphologically and functionally. This paper presents datafrom hatching to 40–52 weeks for a standardised seriesof lungfish, bred at Macquarie University. At hatching, thepineal comprises a single organ attached to the roof of thediencephalon, with well-developed photoreceptor, supportingand ganglion cells. The photoreceptors gradually degenerate,giving way to secretory cells which contain electron dense granules.These latter are immunoreactive to melatonin antibodies anddigestable with protease. The pituitary at hatching comprisesa hollow ball of cells lying beneath the infundibular regionof the hypothalamus. Ultrastructurally, four cell types canbe distinguished by cytoplasmic granule size after the firstfour weeks of development posthatching. By 20 weeks, a furtherthree cell types are recognisable. Inununogold labelling hasidentified corticotropes and melanotropes at four weeks and,at 20 weeks, prolactin cells, thyrotropes and somatotropes alsocan be identified. The thyroid is only just apparent at hatching,containing 2–3 follicles. Thenumbers of follicles increasesgradually, and variably between animals, with age. Iodine uptakein methimazole-treated animals did not exceed that of controlsat any of the three stages tested, indicating a lack of feedbackcontrol between thyroid hormones and pituitary thyrotropes at,or before, 40 weeks of age. Thyroid hormone receptors in theliver at 40 weeks are predominantly immunoreactive to humanTRac antibodies. These findings taken together suggest that,up to 40 weeks post hatching, lungfish development is equivalentto amphibian premetamorphic development. This would be consistentwith lungfish neoteny, but cannot be taken as evidence for neotenyuntil confirmed at later stages of development     

Gene duplication as a major force in evolution

Gene duplication is an important mechanism for acquiring new genes and creating genetic novelty in organisms. Many new gene functions have evolved through gene duplication and it has contributed tremendously to the evolution of developmental programmes in various organisms. Gene duplication can result from unequal crossing over, retroposition or chromosomal (or genome) duplication. Understanding the mechanisms that generate duplicate gene copies and the subsequent dynamics among gene duplicates is vital because these investigations shed light on localized and genomewide aspects of evolutionary forces shaping intra-specific and inter-specific genome contents, evolutionary relationships, and interactions. Based on whole-genome analysis of Arabidopsis thaliana, there is compelling evidence that angiosperms underwent two whole-genome duplication events early during their evolutionary history. Recent studies have shown that these events were crucial for creation of many important developmental and regulatory genes found in extant angiosperm genomes. Recent studies also provide strong indications that even yeast (Saccharomyces cerevisiae), with its compact genome, is in fact an ancient tetraploid. Gene duplication can provide new genetic material for mutation, drift and selection to act upon, the result of which is specialized or new gene functions. Without gene duplication the plasticity of a genome or species in adapting to changing environments would be severely limited. Whether a duplicate is retained depends upon its function, its mode of duplication, (i.e. whether it was duplicated during a whole-genome duplication event), the species in which it occurs, and its expression rate. The exaptation of preexisting secondary functions is an important feature in gene evolution, just as it is in morphological evolution.