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Phenotypic effect of substitutions of short chromosomal segments containing different alleles of histone HI genes in garden pea (Pisum sativum L.)

Published online by Cambridge University Press:  14 April 2009

V. S. Bogdanova ,
S. M. Rozov ,
Y. A. Trusov  and
V. A. Berdnikov
V. S. Bogdanova
Affiliation:
Institute of Cytology and Genetics of SiberianDivision of Russian Academy of Sciences, Academician Lavrentiev Avenue 10, 630090, Novosibirsk, Russia
S. M. Rozov
Affiliation:
Institute of Cytology and Genetics of SiberianDivision of Russian Academy of Sciences, Academician Lavrentiev Avenue 10, 630090, Novosibirsk, Russia
Y. A. Trusov
Affiliation:
Institute of Cytology and Genetics of SiberianDivision of Russian Academy of Sciences, Academician Lavrentiev Avenue 10, 630090, Novosibirsk, Russia
V. A. Berdnikov*
Affiliation:
Institute of Cytology and Genetics of SiberianDivision of Russian Academy of Sciences, Academician Lavrentiev Avenue 10, 630090, Novosibirsk, Russia
*
* Corresponding author
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A hypothesis has been tested that alterations in the molecule of histone H1 are capable of influencing quantitative traits of an organism. Two pairs of isogenic lines were constructed by selfing of plants kept heterozygous either for allelic variants of histone H1 subtype 1 (His1 gene) or for allelic combinations (haplotypes) of closely linked genes of H1 subtypes 3, 4, 5 and 6 (gene cluster His(2–6)). After 19 and 15 generations of selfing, respectively, expectation of the length of chromosome which remained heterozygous has comprised 2·6 cM near Hisl and 3·5 cM near His(2–6). The third pair of isogenic lines was obtained as a result of two successive intracluster cross-over events bordering the gene of the subtype 5 (His5). In each pair of isogenic lines there have been revealed some statistically significant differences between mean values of a number of quantitative traits.

Type
Research Article
Information
Genetics Research , Volume 64 , Issue 1 , August 1994 , pp. 35 - 41
Copyright
Copyright © Cambridge University Press 1994

References

Allan, J., Hartman, P. G., Grane-Robinson, C., & Aviles, F. X., (1980). The structure of histone H1 and its location on chromatin. Nature 288, 675–679.Google Scholar
Belyaev, A. I., & Berdnikov, V. A., (1981). Polymorphism and location of histone HI genes in pea (Pisum sativum L.). Genetika (USSR) 17, 498–504. (in Russian).Google Scholar
Berdnikov, V. A., & Gorel, F. L., (1975). A study of ratios between histone fractions. Molekulyarnaya Biologiya (USSR) 9, 699–705. (in Russian).Google Scholar
Berdnikov, V. A., Rozov, S. M., Temnykh, S. V., Gorel, F. L., & Kosterin, O. E., (1993 a). Adaptive nature of interspecies variation of histone HI in insects. Journal of Molecular Evolution 36, 497–507.Google Scholar
Berdnikov, V. A., Bogdanova, V. S., Rozov, S. M., & Kosterin, O. E. (1993 b). The geographic patterns of histone HI allelic frequencies formed in the course of pea (Pisum sativum L.) cultivation. Heredity 71, 199–209.CrossRefGoogle Scholar
Berdnikov, V. A., Bogdanova, V. S., Gorel, F. L., & Rozov, S. M., (1992). Territorial distribution of histone H1 alleles in a population of Vicia unijuga A.Br. formed after urbanization of natural habitat. Canadian Journal of Botany 70, 1591–1595.Google Scholar
Blixt, S., (1972). Mutation genetics in Pisum. Agri Hortique Genetica 30, 1–293.Google Scholar
Brown, D. D., (1984). The role of stable complexes that repress and activate eukaryotic genes. Cell 37, 359–365.Google Scholar
Johns, E. W., (1964). Studies of histones. 7. Preparative methods for histone fractions from calf thymus. Biochemical Journal 92, 55–59.Google Scholar
Kosterin, O. E., (1992). Mapping of the third locus for histone H1 genes in peas. Pisum Genetics 24, 56–59.Google Scholar
Oikarinen, J., (1991). Histone H1 and the regulation of transcription by nuclear receptors. FEBS Letters 294, 6–10.CrossRefGoogle ScholarPubMed
Panyim, S., & Chalkley, R., (1969). High resolution in acrylamide gel electrophoresis of histones. Archive of Biochemistry and Biophysics 130, 337.Google Scholar
Rozov, S. M., & Berdnikov, V. A., (1982). Determination of lysine residue number, positive charge and molecular length of histones H1 and H5 by an incomplete succinylation method. Biokhimia 47, 1378–1385. (in Russian).Google Scholar
Rozov, S. M., Bogdanova, V. S., & Berdnikov, V. A., (1986). Different chromosomal localizations of genes coding for Pisum histone HI fractions. Genetika (USSR) 22, 2159–2166. (in Russian).Google Scholar
Smirnova, O. G., Rozov, S. M., & Berdnikov, V. A., (1990). New genes linked to r and tl in pea: histone H1 slow fraction and seed albumin K9 genes. Pisum Newsletter 21, 63–65.Google Scholar
Serra, J. A., (1966). Modern Genetics, Vol. 2. London, New York: Academic Press.Google Scholar
Sherod, D., Johnson, G., & Chalkley, R., (1974). Studies on the heterogeneity of lysine-rich histones in dividing cells. Journal of Biological Chemistry 249, 3923.Google Scholar
Thomas, F., Koller, T., & Klug, A., (1979). Involvement of histone HI in the organization of the nucleosome and of the salt-dependent superstructures of chromatin. Journal of Cell Biology 83, 403–421.Google Scholar
Weintraub, H., (1985). Assembly and propagation of repressed and derepressed chromatin states. Cell 42, 705–711.Google Scholar
Wells, D. E., & McBride, C. A., (1989). Comprehensive compilation and alignment of histones and histone genes. Nucleic Acid Research 17. (seq. suppl.), r311–346.Google Scholar
Zlatanova, J., (1990). Histone HI and the regulation of transcription of eukaryotic genes. Trends in Biochemical Science 15, 273–276.Google Scholar