MUTATIONS IN POLYPLOID CEREALS: IV. A SEGMENTAL CHROMOSOME DEFICIENCY DETERMINING AN α SERIES RATIO IN A SPELTOID WHEAT

1951 ◽  
Vol 29 (6) ◽  
pp. 607-630
Author(s):  
Stanley G. Smith

The C chromosome of beardless Triticum vulgare carries epistatic inhibitors, about 30 crossover units apart on the longer arm of the chromosome, which prevent the expression of the bearded-speltoid complex of genes. It has earlier been shown that het speltoid mutants may lack one of the two sets of inhibitors through the loss of the entire C chromosome, or its longer arm, or an interstitial segment of this arm. The first determines Series β segregation (1 normal: ca. 5 het speltoids: ca. 0.03 speltoids), the last two Series γ (1: 1: ca. 0.05). A third type of progeny ratio, α, is a distortion of a 1: 2: 1 caused by a greater or lesser deficiency of speltoids and, less markedly, of het speltoids. Some workers regard α ratios as resulting from mutation of the epistatic inhibitors to their recessive state; others as due to chromosome aberration similar to, but less extensive than, that observed in typical γ strains. The latter interpretation is proved correct herein. That deviations from the ratios characteristic of the three Series are determined by the degree of pollen certation superimposed on the proportion in which normal and mutant ovules are formed has been shown by analyses involving natural hybrids and crosses made with other types. The extent of certation in α and γ Series may be measured from their progeny ratios—normal pollen = N + H − Sp: mutant pollen = 2 × Sp. A rough correlation has been established between the length of the mutant C chromosome, percentage conjugation with C, proportion of N: Sp progeny, percentage β het Sp progeny, and the coefficient of certation. The percentage het Sp of Series β expected as secondary mutants in the het Sp progeny of α and γ het Sp approximates to [Formula: see text].

1952 ◽  
Vol 30 (1) ◽  
pp. 40-49 ◽  
Author(s):  
R. C. McGinnis ◽  
John Unrau

Meiosis was studied in the haploid of Triticum vulgare and in its second and third generation selfed progenies derived from pollination of the haploid with normal pollen. In the haploid, 57.6% of the metaphase cells showed one to three bivalents. This is assumed to be evidence of a degree of homology between chromosomes of the haploid set. Random distribution of univalents to the poles was apparently restricted by bivalent and secondary associations. Cells with 42 chromosomes were observed in a few instances. In one case the complement was made up of 21 bivalents. A high frequency of trivalents and quadrivalents was observed in the second and third generations. Presumably crossing over between partially homologous chromosomes, occurring in the haploid, resulted in reciprocal translocations which were transmitted to succeeding generations. Plants with chromosomal deficiency or duplication, observed in the second and third generations, probably originated from union of unbalanced gametes in first generation plants heterozygous for translocations or deficient or duplicated for one or more chromosomes.


2020 ◽  
Vol 16 (7) ◽  
pp. 1072-1082
Author(s):  
Tuba C. Dördü ◽  
Rüştü Hatipoğlu ◽  
Mehmet Topaktaş ◽  
Erman S. İstifli

Background: Ellagic Acid (EA) is a polyphenolic compound that is classified in the natural antioxidants group. Polyphenolic compounds that exert antioxidant activity possess particular importance for scientists, food producers and consumers due to their positive effects on human health. However, despite considerable evidence that EA shows antigenotoxic activity by binding to DNA, there is no systematic genotoxicity study of this substance, which can covalently bind to DNA. This study aims to reveal the possible genotoxic activity of EA using widely accepted assays for the assessment of DNA clastogenic activity: sister chromatid exchange, chromosome aberration, micronucleus and comet assays as well as to predict the interactions among EA and DNA through molecular docking. Methods: Different assays were carried out to identify the clastogenic activity of EA on human lymphocyte DNA using Sister Chromatid Exchange (SCE), Chromosome Aberration (CA), Micronucleus (MN) and single-cell gel electrophoresis (SCGE/comet) assays. For this aim, human peripheral blood lymphocytes were treated with EA (60, 80 and 100 μg/ml) for 24 and 48 hrs in the SCE, CA and MN assays and for 1 hr in the comet assay. Furthermore, molecular docking experiments were also performed to calculate the binding energy of EA on human B-DNA structure (B-DNA dodecamer) as well as to predict noncovalent interactions among these macromolecules. Results: At the concentrations and treatment times (24- or 48-hr) tested, EA did not induce either SCE or Chromosome Aberrations (CAs) as compared to the negative and solvent controls. Although EA slightly increased the percentage of Micronucleated Binuclear (%MNBN) cells as well as the percentage of Micronucleus (%MN) in 24 or 48-hr treatment periods at all concentrations, this increase was not statistically significant as compared to both controls. The effect of EA on DNA replication (nuclear division) was determined by the Proliferation Index (PI), the Nuclear Division Index (NDI) and the Mitotic Index (MI). No statistically significant differences were observed in the PI or NDI in 24- or 48-hr treatment periods in human lymphocyte cultures treated with EA at various concentrations. EA generally had no significant effect on the MI, as observed with the PI and NDI. Discussion: Although the concentrations of 60 and 80 μg/mL at a 24-hr treatment period and the concentrations of 60 μg/mL and 100 μg/mL at 48-hr treatment period generally decreased the MI, those decreases were not statistically significant when compared to negative and solvent controls. Moreover, none of the concentrations of EA tested in this study were able to increase DNA damage determined by the tail DNA length, %DNA in tail and tail moment parameters in the comet assay. Although the amount of DNA damage in the comet assay decreased with increasing concentrations of EA, this decrease was not statistically significant as compared to both controls. However, molecular docking experiments interestingly showed that the binding free energy of EA with B-DNA was -7.84 kcal/mol-1, indicating a strong interaction between the two molecules. Conclusion : Although the findings of our study show that EA does not have genotoxic potential in human chromosomes, molecular docking experiments revealed strong hydrogen bonding between EA and B-DNA molecules. Therefore, it has been proposed that the prevailing information suggesting that the molecules that bind to DNA cause genotoxic effects should be reconsidered from a wider perspective.


Biology ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 290
Author(s):  
Abdul Kader Alabdullah ◽  
Graham Moore ◽  
Azahara C. Martín

Although most flowering plants are polyploid, little is known of how the meiotic process evolves after polyploidisation to stabilise and preserve fertility. On wheat polyploidisation, the major meiotic gene ZIP4 on chromosome 3B duplicated onto 5B and diverged (TaZIP4-B2). TaZIP4-B2 was recently shown to promote homologous pairing, synapsis and crossover, and suppress homoeologous crossover. We therefore suspected that these meiotic stabilising effects could be important for preserving wheat fertility. A CRISPR Tazip4-B2 mutant was exploited to assess the contribution of the 5B duplicated ZIP4 copy in maintaining pollen viability and grain setting. Analysis demonstrated abnormalities in 56% of meiocytes in the Tazip4-B2 mutant, with micronuclei in 50% of tetrads, reduced size in 48% of pollen grains and a near 50% reduction in grain number. Further studies showed that most of the reduced grain number occurred when Tazip4-B2 mutant plants were pollinated with the less viable Tazip4-B2 mutant pollen rather than with wild type pollen, suggesting that the stabilising effect of TaZIP4-B2 on meiosis has a greater consequence in subsequent male, rather than female gametogenesis. These studies reveal the extraordinary value of the wheat chromosome 5B TaZIP4-B2 duplication to agriculture and human nutrition. Future studies should further investigate the role of TaZIP4-B2 on female fertility and assess whether different TaZIP4-B2 alleles exhibit variable effects on meiotic stabilisation and/or resistance to temperature change.


2009 ◽  
Vol 25 (7) ◽  
pp. 467-471 ◽  
Author(s):  
BN Mojidra ◽  
K. Archana ◽  
AK Gautam ◽  
Y. Verma ◽  
BC Lakkad ◽  
...  

Pan masala is commonly consumed in south-east Asian and other oriental countries as an alternate of tobacco chewing and smoking. Genotoxic potential of pan masala (pan masala plain and pan masala with tobacco known as gutkha) was evaluated employing chromosome aberration (CA) and micronucleus (MN) assay in vivo. Animals were exposed to three different doses (0.5%, 1.5% and 3%) of pan masala plain (PMP) and gutkha (PMT) through feed for a period of 6 months and micronucleus and chromosomal aberrations were studied in the bone marrow cells. Induction of mean micronuclei in polychromatic erythrocytes (MNPCE) and normochromatic erythrocyte (MNNCE) was higher in both types of pan masala treated groups with respect to control group. Both pan masala plain and gutkha treatment significantly induced the frequency of MNPCE and MNNCE in the bone marrow cells, indicating the genotoxic potential. Furthermore, slight decline in the ratio of polychromatic erythrocytes to normochromatic erythrocytes was also noticed, suggesting the cytotoxic potential even though the ratio was statistically non significant. A dose-dependent, significant increase in chromosome aberration was observed in both types of pan masala treated mice with respect to control. However, no significant difference in micronucleus and chromosomal aberration induction was noticed between two types of pan masala exposed (PMP and PMT) groups. Results suggest that both types of pan masala, i.e. plain and gutkha, have genotoxic potential.


1946 ◽  
Vol 24c (3) ◽  
pp. 66-73 ◽  
Author(s):  
Raymond J. Moore

The chromosome number of eight species and varieties of Asclepias (A. syriaca, A. incarnata and variety pulchra and forma albiflora, A. Sullivantii, A. tuberosa, A. curassavica, A. speciosa) was found to be 2n = 22.Various interspecific pollinations were attempted without success. A cross of A. incarnata with forma albiflora was successful.Possible natural hybrids between A. syriaca and A. speciosa and between A. incarnata and var. pulchra and forma albiflora are described. Two unusual chimaeral plants of A. incarnata that produced several stems of forma albiflora are described.


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