1987
DOI: 10.1139/g87-073
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A separate control for frequency and within-bivalent distribution of chiasmata in rye (Secale cereale L.)

Abstract: LEIN, V., and LELLEY, T. 1987. A separate control for frequency and within-bivalent distribution of chiasmata in rye (Secale cereale L.). Genome, 29: 4 19-424. Six genetically different inbred genotypes of spring-type rye Secale cereale with differences in the average number and in the positional distribution of chiasmata were used in this study. The line with the lowest chiasma frequency was chosen as the female parent and crossed with the other five lines. Parental, F, , and F2 data were collected on chiasma… Show more

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Cited by 11 publications
(10 citation statements)
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“…These authors did not find any bivalents with one chiasma, whereas we detected a mean of 5.45 bivalents among the fourteen present in each microsporocyte, with only one chiasma and more than a half of these (M=2.92) showing a terminal chiasma. Since chiasma frequency (Rees and Thompson 1958, Pagliarini 1980, Karp and Jones 1982, Lein and Lelley 1987 and chiasma distribution (Jones 1967, Karp and Jones 1983, Lein and Lelley 1987 are under genetic control, the difference between the plants analysed here and the plants analysed by Patil and Gandhi (1988) could be of a genetic nature. Absence of chiasma and precocious chiasma terminalization have been reported to be respon sible for the occurrence of univalents in maize (Pagliarini 1980(Pagliarini , 1989, Aptenia cordifolia (Pagliarini 1990), and Pilocarpus pennatifolius (Pagliarini and Pereira 1992).…”
Section: Discussionmentioning
confidence: 87%
“…These authors did not find any bivalents with one chiasma, whereas we detected a mean of 5.45 bivalents among the fourteen present in each microsporocyte, with only one chiasma and more than a half of these (M=2.92) showing a terminal chiasma. Since chiasma frequency (Rees and Thompson 1958, Pagliarini 1980, Karp and Jones 1982, Lein and Lelley 1987 and chiasma distribution (Jones 1967, Karp and Jones 1983, Lein and Lelley 1987 are under genetic control, the difference between the plants analysed here and the plants analysed by Patil and Gandhi (1988) could be of a genetic nature. Absence of chiasma and precocious chiasma terminalization have been reported to be respon sible for the occurrence of univalents in maize (Pagliarini 1980(Pagliarini , 1989, Aptenia cordifolia (Pagliarini 1990), and Pilocarpus pennatifolius (Pagliarini and Pereira 1992).…”
Section: Discussionmentioning
confidence: 87%
“…Table 1 presents the frequency of affected cells. Besides the polygenes controlling the chiasma frequency (Rees and Thompson, 1956;Lein and Lelley, 1987), two other categories of genes can affect synapsis. The asynaptic genes hinder chromosome pairing (Gottschalk and Kaul, 1980a) while the desynaptic genes promote desynapsis in bivalents before metaphase I (Gottschalk and Kaul, 1980b).…”
Section: Resultsmentioning
confidence: 99%
“…In maize (Zea mays L.), the frequency of chiasmata is under polygenic control, which may lead to genetic variability in lineages (Pagliarini 1980). The polygenic chiasma control has also been demonstrated in rye, Secale cerale (Rees & Thompson 1958, Lein & Lelley 1987. The formation of chiasmata is a good characteristic, since it ensures the genetic variability of plants, thus having a direct influence on the adaptation mechanisms.…”
Section: Discussionmentioning
confidence: 96%