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A behavior of chromosomes 6R and 6A at the late anaphase II of meiosis. (a)-single chromatids nonnincluded into nuclei. (b)-chromatid located across the equator during the fragmoplast formation. 

A behavior of chromosomes 6R and 6A at the late anaphase II of meiosis. (a)-single chromatids nonnincluded into nuclei. (b)-chromatid located across the equator during the fragmoplast formation. 

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The effect of wheat-rye chromosome 1Rv/1A, 2R/2D and 6R/6A substitutions characterized by differences in the expression of the equational division of sister centromeres in anaphase I on segregation and the elimination of wheat and rye univalents was investigated. To determine the individual effect of each of the studied chromosomal pairs, a compara...

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... reveal the individual impact of each of the inves tigated chromosomal pairs, a comparison of the univa lent chromosomal behavior in the meiosis of dii and tetramonosomics was conducted. Univalent chromosomal behavior in the meiosis of dimonosomics 1Rvv1A, 2RR2D, 6RR6A. Each PMC analyzed at the MI stage was characterized by the presence of two univalents in dimonosomics: rye and wheat chromosomes. Univalent chromosomes were located randomly near the cell poles or on the equatoo rial plane, together with bivalents ( Fig. 2a). Subsee quently, both univalents segregated simultaneously with bivalents at stage AI (Fig. 2b) or were detained on the cell equator (Fig. 2c). The last ones divided on the siss ter chromatids and segregated to opposite poles (Fig. 2d). Such univalent behavior was unobserved in all meioo cytes. An equatorial delay did not always result in the division into sister chromatids, the segregation of divided chromatids to the poles (Fig. 2e) or transversal division of one of chromatids (Fig. 2f). The second division was characterized by chromatid delay on the equator after the segregation of all chromosomes until late anaphase II (Fig. 3a) and the presence of single chromatids across the equator during fragmoplast forr mation (Fig. 3b). Such behavior resulted in their nonn inclusion into microspores nuclei. In the present experiment, we considered meiocytes in AI with unii valent chromosomes divided into sister chromatids and with chromatids segregated to the poles, i.e. an equational division ...
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... reveal the individual impact of each of the inves tigated chromosomal pairs, a comparison of the univa lent chromosomal behavior in the meiosis of dii and tetramonosomics was conducted. Univalent chromosomal behavior in the meiosis of dimonosomics 1Rvv1A, 2RR2D, 6RR6A. Each PMC analyzed at the MI stage was characterized by the presence of two univalents in dimonosomics: rye and wheat chromosomes. Univalent chromosomes were located randomly near the cell poles or on the equatoo rial plane, together with bivalents ( Fig. 2a). Subsee quently, both univalents segregated simultaneously with bivalents at stage AI (Fig. 2b) or were detained on the cell equator (Fig. 2c). The last ones divided on the siss ter chromatids and segregated to opposite poles (Fig. 2d). Such univalent behavior was unobserved in all meioo cytes. An equatorial delay did not always result in the division into sister chromatids, the segregation of divided chromatids to the poles (Fig. 2e) or transversal division of one of chromatids (Fig. 2f). The second division was characterized by chromatid delay on the equator after the segregation of all chromosomes until late anaphase II (Fig. 3a) and the presence of single chromatids across the equator during fragmoplast forr mation (Fig. 3b). Such behavior resulted in their nonn inclusion into microspores nuclei. In the present experiment, we considered meiocytes in AI with unii valent chromosomes divided into sister chromatids and with chromatids segregated to the poles, i.e. an equational division ...

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... Most of the studies performed during meiosis in wheat plants carrying alien chromosomes are focused on meiosis metaphase I or later stages [35,46,47]. Previously, we studied interspecific chromosome associations in early meiosis stages (pachytene) and we managed to track simultaneously extra wild and cultivated barley chromosomes (for the same and for different homoeology groups) in the wheat background using in situ hybridization [21]. ...
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