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Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye. / Sosnikhina, S. P.; Mikhailova, E. I.; Tikholiz, O. A.; Tsvetkova, N. V.; Lovtsyus, A. V.; Sapronova, O. S.; Fedotova, Yu S.; Kolomiets, O. L.; Bogdanov, Yu F.

в: Russian Journal of Genetics, Том 43, № 10, 01.10.2007, стр. 1193-1200.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Sosnikhina, SP, Mikhailova, EI, Tikholiz, OA, Tsvetkova, NV, Lovtsyus, AV, Sapronova, OS, Fedotova, YS, Kolomiets, OL & Bogdanov, YF 2007, 'Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye', Russian Journal of Genetics, Том. 43, № 10, стр. 1193-1200. https://doi.org/10.1134/S1022795407100146

APA

Sosnikhina, S. P., Mikhailova, E. I., Tikholiz, O. A., Tsvetkova, N. V., Lovtsyus, A. V., Sapronova, O. S., Fedotova, Y. S., Kolomiets, O. L., & Bogdanov, Y. F. (2007). Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye. Russian Journal of Genetics, 43(10), 1193-1200. https://doi.org/10.1134/S1022795407100146

Vancouver

Sosnikhina SP, Mikhailova EI, Tikholiz OA, Tsvetkova NV, Lovtsyus AV, Sapronova OS и пр. Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye. Russian Journal of Genetics. 2007 Окт. 1;43(10):1193-1200. https://doi.org/10.1134/S1022795407100146

Author

Sosnikhina, S. P. ; Mikhailova, E. I. ; Tikholiz, O. A. ; Tsvetkova, N. V. ; Lovtsyus, A. V. ; Sapronova, O. S. ; Fedotova, Yu S. ; Kolomiets, O. L. ; Bogdanov, Yu F. / Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye. в: Russian Journal of Genetics. 2007 ; Том 43, № 10. стр. 1193-1200.

BibTeX

@article{207b4250897342f1961f4c673ecd1e9e,
title = "Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye",
abstract = "The cytological phenotype was studied in a desynaptic form isolated from a population of rye cultivar Vyatka. The primary defect of desynaptic plants was identified as nonhomologous (heterologous) chromosome synapsis, which was observed by electron microscopy of synaptonemal complexes (SCs) in meiotic prophase I. Synapsis defects involved switches of synapsing axial elements to nonhomologous partners, asynapsis in the switching region, and foldbacks formed by the SC lateral elements. Defective bivalent formation was observed at later stages: the univalent number varied and multivalent chromosome associations were observed in single cells in metaphase I. The desynaptic phenotype was controlled by two recessive genes, sy8a and sy8b, which acted and were inherited independently. In a hybrid combination with line Ku-2/63, the desynaptic phenotype was suppressed by the dominant allele of a third gene for inhibitor I; the segregation in hybrid families corresponded to 57:7.",
author = "Sosnikhina, {S. P.} and Mikhailova, {E. I.} and Tikholiz, {O. A.} and Tsvetkova, {N. V.} and Lovtsyus, {A. V.} and Sapronova, {O. S.} and Fedotova, {Yu S.} and Kolomiets, {O. L.} and Bogdanov, {Yu F.}",
year = "2007",
month = oct,
day = "1",
doi = "10.1134/S1022795407100146",
language = "English",
volume = "43",
pages = "1193--1200",
journal = "Russian Journal of Genetics",
issn = "1022-7954",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "10",

}

RIS

TY - JOUR

T1 - Expression and Inheritance of a desynaptic phenotype with impaired homologous synapsis in rye

AU - Sosnikhina, S. P.

AU - Mikhailova, E. I.

AU - Tikholiz, O. A.

AU - Tsvetkova, N. V.

AU - Lovtsyus, A. V.

AU - Sapronova, O. S.

AU - Fedotova, Yu S.

AU - Kolomiets, O. L.

AU - Bogdanov, Yu F.

PY - 2007/10/1

Y1 - 2007/10/1

N2 - The cytological phenotype was studied in a desynaptic form isolated from a population of rye cultivar Vyatka. The primary defect of desynaptic plants was identified as nonhomologous (heterologous) chromosome synapsis, which was observed by electron microscopy of synaptonemal complexes (SCs) in meiotic prophase I. Synapsis defects involved switches of synapsing axial elements to nonhomologous partners, asynapsis in the switching region, and foldbacks formed by the SC lateral elements. Defective bivalent formation was observed at later stages: the univalent number varied and multivalent chromosome associations were observed in single cells in metaphase I. The desynaptic phenotype was controlled by two recessive genes, sy8a and sy8b, which acted and were inherited independently. In a hybrid combination with line Ku-2/63, the desynaptic phenotype was suppressed by the dominant allele of a third gene for inhibitor I; the segregation in hybrid families corresponded to 57:7.

AB - The cytological phenotype was studied in a desynaptic form isolated from a population of rye cultivar Vyatka. The primary defect of desynaptic plants was identified as nonhomologous (heterologous) chromosome synapsis, which was observed by electron microscopy of synaptonemal complexes (SCs) in meiotic prophase I. Synapsis defects involved switches of synapsing axial elements to nonhomologous partners, asynapsis in the switching region, and foldbacks formed by the SC lateral elements. Defective bivalent formation was observed at later stages: the univalent number varied and multivalent chromosome associations were observed in single cells in metaphase I. The desynaptic phenotype was controlled by two recessive genes, sy8a and sy8b, which acted and were inherited independently. In a hybrid combination with line Ku-2/63, the desynaptic phenotype was suppressed by the dominant allele of a third gene for inhibitor I; the segregation in hybrid families corresponded to 57:7.

UR - http://www.scopus.com/inward/record.url?scp=35349031212&partnerID=8YFLogxK

U2 - 10.1134/S1022795407100146

DO - 10.1134/S1022795407100146

M3 - Article

AN - SCOPUS:35349031212

VL - 43

SP - 1193

EP - 1200

JO - Russian Journal of Genetics

JF - Russian Journal of Genetics

SN - 1022-7954

IS - 10

ER -

ID: 49678693