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Embryonic development results in animals whose body plans exhibit a variety of symmetry types. While significant progress has been made in understanding the molecular events underlying the early specification of the antero-posterior and dorso-ventral axes, little information has been available regarding the basis for left-right (LR) differences in animal morphogenesis. Recently however, important advances have been made in uncovering the molecular mechanisms responsible for LR patterning. A number of genes (including well-known signaling molecules such as Sonic hedgehog and activin) are asymmetrically expressed in early chick embryos, well before the appearance of morphological asymmetries. One of these, nodal, is asymmetrically expressed in frogs and mice as well, and its expression is altered in mouse mutants exhibiting defects in laterality. In the chick, these genes regulate each other in a sequential cascade, which independently determines the situs of the heart and other organs.
Embryonic development results in animals whose body plans exhibit a variety of symmetry types. While significant progress has been made in understanding the molecular events underlying the early specification of the antero-posterior and dorso-ventral axes, little information has been available regarding the basis for left-right (LR) differences in animal morphogenesis. Recently however, important advances have been made in uncovering the molecular mechanisms responsible for LR patterning. A number of genes (including well-known signaling molecules such as Sonic hedgehog and activin) are asymmetrically expressed in early chick embryos, well before the appearance of morphological asymmetries. One of these, nodal, is asymmetrically expressed in frogs and mice as well, and its expression is altered in mouse mutants exhibiting defects in laterality. In the chick, these genes regulate each other in a sequential cascade, which independently determines the situs of the heart and other organs.
Gastrulae (Harrison 9-13), and for comparison neurulae (Harrison 15-17) ofTriturus alpestris were irradiated with mixed ultraviolet light of various doses and at various body regions. Bilateral irradiation leads to a markedly higher mortality than does unilateral irradiation. Gastrulae possess a better regulation capability than neurulae. The frequency of alterations of the situs (irregularities, partial and total inversions), lethality and rate of malformations are dose dependent. Irradiation of the right side ofearly gastrulae (Harrison 9-11a) leads to a higher frequency of inversions than does irradiation of the left or animal side. The frequency of inversions oflater gastrulae (Harrison 12-13) is approximately the same after right- and left-side irradiation. The expressions of inversions are different after irradiation of gastrulae and of neurulae respectively. The problem of physiological asymmetry of the embryo, especially the change of "dominance for right" to "dominace for left" during gastrulation is discussed with regard of relations of defect and situs inversions.
1. Of 10,695 larvae ofTriturus alpestris, 419 exhibitedcomplete orincomplete situs inversus in at least one of their asymmetric organs, i.e.alimentary canal, heart, andnuclei habenulae. The abnormal (nonregular) animals appeared in the following groups: a) 33 (0.9% of 3,801) among the control animals (spontaneous reversal), b) 50 (2.6% of 1,947) in a series in which the eggs were not stripped from the grass leaves to which they had been attached ("blade series"). c) 83 (3% of 2,748) afterx-irradiation between cleavage and late neurulation. d) 253 (of 2,199) after exposure tolithium sulfate hydrate between the morula and early postneurula stages. Thus x-irradiation and particularly lithium treatment proved capable of provoking situs inversus. These two nonsurgical methods were most effective when applied at the gastrula stage. 2. The asymmetric organs were completely or incompletely reversed. Thevarious degrees of reversal formed graded series of reactions ranging from almost normal situs to ideal situs inversus. In 65% of the nonregular larvae, all three organs were nonregular. The three did not differ in the faculty of assuming the reversed state. In each of them, incomplete reversal occurred more frequently than complete reversal, and incompletely reversed larvae outnumbered the completely reversed by, for example, 73∶27 in the control group or 88∶12 in the lithium series. The several grades of reversal of the three organs were combined in almost any conceivable way; the anlagen are obviously capable of responding independently of one another. Nonetheless, in most cases gut, heart, and habenulae reacted jointly and similarly. 3. InTriturus, no convincing evidence for monohybrid inheritance of spontaneous reversal is available. A polygenic basis to account for the lability of sidedness is discussed. 4. There was no direct relationship between the larval malformations (e.g. flexures of the body) caused by x-irradiation or lithium treatment and the occurrence of reversal. 5. Presumably, a microstructure that is asymmetric in itself and capable of determining the orientation of the asymmetric organs is present in the egg and transmitted to all rudiments so that each of them possesses an intrinsic orienting tendency. Reversal is probably an incidental effect of the disturbance of normal development. Surgical methods, such as replantation, constriction, or extirpation, and nonsurgical methods, such as x-irradiation or lithium treatment, provoke regulatory movements, in the course of which the anlagen are rearranged. The rudiments may become rotated with respect to their original orientations, and their intrinsic microstructures may therefore assume abnormal relative positions to the geometrical axes of the embryo. This change in the relative positions is the direct cause of situs inversus, the degree of reversal depending on the angle of rotation. In the small egg, the three organs are often affected similarly, though the looseness of the connections between the rearranging cell complexes permits local differences in...
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