Revisiting the Hetero-Fertilization Phenomenon in Maize

Development of a seed DNA-based genotyping system for marker-assisted selection (MAS) has provided a novel opportunity for understanding aberrant reproductive phenomena such as hetero-fertilization (HF) by observing the mismatch of endosperm and leaf genotypes in monocot species. In contrast to conventional approaches using specific morphological markers, this approach can be used for any population derived from diverse parental genotypes. A large-scale experiment was implemented using seven F2 populations and four three-way cross populations, each with 534 to 1024 individuals. The frequency of HF within these populations ranged from 0.14% to 3.12%, with an average of 1.46%. The highest frequency of HF in both types of population was contributed by the pollen gametes. Using three-way crosses allowed, for the first time, detection of the HF contributed by maternal gametes, albeit at very low frequency (0.14%–0.65%). Four HF events identified from each of two F2 populations were tested and confirmed using 1032 single nucleotide polymorphic markers. This analysis indicated that only 50% of polymorphic markers can detect a known HF event, and thus the real HF frequency can be inferred by doubling the estimate obtained from using only one polymorphic marker. As expected, 99% of the HF events can be detected by using seven independent markers in combination. Although seed DNA-based analysis may wrongly predict plant genotypes due to the mismatch of endosperm and leaf DNA caused by HF, the relatively low HF frequencies revealed with diverse germplasm in this study indicates that the effect on the accuracy of MAS is limited. In addition, comparative endosperm and leaf DNA analysis of specific genetic stocks could be useful for revealing the relationships among various aberrant fertilization phenomena including haploidy and apomixis

The relation of a particular chromosomal element to the development of the nucleoli in Zea mays

1.The nucleolus is organized in the telophase through the activity of a distinct deep-staining body having a definite position in one chromosome (the satellited chromosome) of the monoploid complement. Correlated with the number of satellited chromosomes present, the telophases of somatic tissue of haploids show one nucleolus, diploids, two nucleoli and triploids, three nucleoli. That the nucleolus develops through the activity of this body (refered to as the nucleolar-organizing body or element) was obtained from a reciprocal translocation which broke this body into two parts. Both interchanged chromosomes possessed a section. Nucleoli developed from each of these two segments. Thus, plants homozygous for the interchange developed four nucleoli in their somatic telophases; plants heterozygous for the interchange developed three nucleoli in their somatic telophases. Similarly, the telophase nucleoli resulting from the first division within the monoploid microspore of normal diploids show only one nucleolus, whereas, those of plants homozygous for the interchange are characterized by the development of two nucleoli. 2.The functional capacity to develop a nucleolus is not the same for both segments of the severed nucleolar-organizing body. This is evident when the two interchanged chromosomes are present in the same nucleus. The segment of the nucleolar-organizing body possessed by one interchanged chromosome produced a large nucleolus, whereas, the segment of the nucleolar-organizing body possessed by the other interchanged chromosome produced a small nucleolus. When this latter chromosome, with the nucleolar-organizing element of slower rate of functional capacity is present without the former (i. e. without a competing nucleolarorganizing element) it produces, in contrast, a large nucleolus. 3.The activity of the nucleolar-organizing element is hindered by certain genomic deficiencies. When this occurs, many small nucleolarlike bodies are produced and remain associated with the other chromosomes of the complement. These small nucleoli appear to develop from a swelling and later collection into droplets of the matrix substance of the chromosome