N S Fechheimer’s research while affiliated with The Ohio State University and other places

Gonadal histological analysis was conducted on 7 pure triploid White Leghorn chicken embryos and 1 2n/3n chimera at d 13 of incubation. Triploid embryos with sex chromosome complements ZZZ and ZWW exhibited gonadal organization consistent with that of normal diploid embryos while that of the ZZW triploid embryo was consistent with adult intersex birds. The morphology of the testes of the 5 ZZZ triploids resembled that of normal ZZ males. The right and left ovaries of the ZWW triploid embryo were similar histologically to those of normal diploid ZW females. The intersex ZZW triploid and ZW/ZZW chimera exhibited normal left ovarian organization but the right ovaries contained testis-like structures, similar to the reported histology of right ovaries in adult ZZW birds. The deviation of the observed numbers of each type of triploid embryos at d 13 of incubation from the expected number based on previous observations of embryos at 16 to 18 h of incubation suggests differential mortality for the 3 types of triploid embryos.

A mitotic anomaly, unlike any previously reported, was observed in all cells of 20 early embryos from five full-sib families from a Japanese quail population subjected to full-sib mating for three generations. The anomaly is characterized by chromosomes that were not attached at the centromere region, similar to premature centromere division. The ratio of nonaffected to affected embryos, in families with at least one affected embryo, was not significantly different from 3:1 ( P < .50), which suggests that the anomaly is autosomal recessive. The putative gene responsible is designated mit -1.

The Japanese quail was used as an experimental system to detect the effects of genes that affect chromosome behavior and distribution. From a random-bred population, three inbred generations were produced by full-sib matings in 36 families. The expectation from such a breeding scheme was that embryos bearing aberrations induced by recessive mutant genes would cluster within families and recur in particular lineages. Chromosomal aberrations caused by errors during fertilization, cleavage mitosis, and gametogenesis were scored in 2,037 16- to 18-h embryos from 107 families. Comparisons of the observed frequencies among families and lineages and pedigree analysis indicated that four types of chromosome aberrations had a genetic basis: (1) triploidy and triploid chimerism; (2) haploidy and haploid chimerism; (3) diploid/tetraploid mosaicism; and (4) a new aberration, referred to as "atypical mitotic metaphase." Analysis of the sex-chromosome complements of the embryos indicated that triploidy resulted predominantly from diploid ova, haploid cell lines originated from supernumerary sperm nuclei, and tetraploid cell lines resulted from endoreduplication or failure of cytokinesis. Clustering of triploidy in particular lineages was due to dispermy or recurrent suppression of one or both meiotic divisions during oogenesis.

Observations were made of the C-banding patterns in several cells from 182 Japanese quail embryos to detect presence of stable variants. Each of the eight largest autosomes contains a C-band at the centromeric region. The short arm of autosome 8 is C-band positive, as is the entire W chromosome. The Z chromosome consistently contains an interstitial C-band in the long arm and a less prominent one in the short arm. Distinct variants of chromosome 4 and the Z chromosome were observed. In the Z chromosome a C-band at the terminal region of the short arm was markedly elongated in some embryos. Likewise, the short arm of chromosome 4 was much more prominent in one or both of the homologues in some embryos. Most of the microchromosomes contain a prominent C-band. The heteromorphisms are useful chromosome markers to detect the origins of heteroploidy in early embryos.

A high incidence of haploid/diploid chimerism in chick embryos from strains of chickens selected for large size was postulated to be caused by the propensity of such hens to ovulate erratically. To test the hypothesis karyological analysis was made of embryos in eggs containing 1 or greater than 1 yolk. The eggs were from a line selected for multiple ovulation for 20 generations. Double and multiple-yolk eggs are a manifestation of an irregular ovulatory pattern. Ova in multiple yolk eggs were significantly less fertile and significantly fewer embryos survived to 18 h of incubation than single ovulated ova. In the sample of 342 embryos analysed, only 2 forms of heteroploidy occurred in frequencies of greater than 1.2%; 2n/4n mosaicism (5.8%) and 3n (5.0%). Only triploidy occurred significantly more frequently in eggs containing greater than 1 yolk (7.0%) than in single yolk eggs (none). The overwhelming majority of 3n embryos had a digynic origin (i.e from ova with 2 maternal pronuclei), as inferred from the sex chromosome complement. Erratic ovulation therefore resulted in suppression of second polar body extrusion leading to digynic triploidy. Multiple yolks had no effect on dispermy, the primary cause of 1n/2n chimaeric embryos, in single-yolked chicken eggs.

Synaptonemal complex analysis of an exceptional tetraploid oocyte from a diploid chicken heterozygous for the MN t (Z;1) rearrangement was performed by electron microscopy of a spread preparation. Ten separate quadrivalents (26% of the chromosomal axes) were analyzed, as well as 50 autosomal bivalents. All the axes less than 2.5 microns in length formed bivalents (38) only, while axes in the 2.5-4.2 micron range formed 5 quadrivalents and 12 bivalents. The longer, separate axes formed quadrivalents only. Partner switches in excess of one were documented. The two identical W chromosomes paired only at the ends of their short arms. Quadrivalent formation may require a threshold length (2.5 microns), at least in this species. The tip of the short arm of the W chromosome may be a pairing initiation point, and it corresponds to the region associated with a localized recombination nodule previously described in diploid oocytes.