The role of the genome in the development of the haploid syndrome in Anura
The problem of the factors involved in the development of the haploid syndrome in anuran embryos is as yet unsolved. It is known that about 90 % of all haploid frog embryos develop the haploid syndrome, which is characterized by the presence of oedema and sluggishness, by reduction in pigmentation and in the efficiency of the heart and circulation, and by a partial failure of the gut to coil and of muscle to differentiate. The two most favoured explanations of the development of the haploid syndrome have been nucleocytoplasmic imbalance, since a haploid nucleus is only half the size of a diploid nucleus in the same-sized egg, and unmasked recessive lethal genes. There is good evidence that an abnormal nucleocytoplasmic ratio is an important contributory factor in the development of the haploid syndrome. Briggs (1949) compared populations of haploids developing from large and small eggs and Subtelny (1958) compared the development of haploids and homozygous diploids which possessed a reduplicated set of haploid chromosomes.