Skip to main content
Genetics logoLink to Genetics
. 1998 Nov;150(3):1229–1237. doi: 10.1093/genetics/150.3.1229

Interchromosomal recombination in Zea mays.

W Hu 1, M C Timmermans 1, J Messing 1
PMCID: PMC1460381  PMID: 9799274

Abstract

A new allele of the 27-kD zein locus in maize has been generated by interchromosomal recombination between chromosomes of two different inbred lines. A continuous patch of at least 11,817 bp of inbred W64A, containing the previously characterized Ra allele of the 27-kD zein gene, has been inserted into the genome of A188 by a single crossover. While both junction sequences are conserved, sequences of the two homologs between these junctions differ considerably. W64A contains the 7313-bp-long retrotransposon, Zeon-1. A188 contains a second copy of the 27-kD zein gene and a 2-kb repetitive element. Therefore, recombination results in a 7.3-kb insertion and a 14-kb deletion compared to the original S+A188 allele. If nonpairing sequences are looped out, 206 single base changes, frequently clustered, are present. The structure of this allele may explain how a recently discovered example of somatic recombination occurred in an A188/W64A hybrid. This would indicate that despite these sequence differences, pairing between these alleles could occur early during plant development. Therefore, such a somatically derived chimeric chromosome can also be heritable and give rise to new alleles.

Full Text

The Full Text of this article is available as a PDF (198.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Athma P., Peterson T. Ac induces homologous recombination at the maize P locus. Genetics. 1991 May;128(1):163–173. doi: 10.1093/genetics/128.1.163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baltimore D. Somatic mutation gains its place among the generators of diversity. Cell. 1981 Nov;26(3 Pt 1):295–296. doi: 10.1016/0092-8674(81)90196-3. [DOI] [PubMed] [Google Scholar]
  3. Borts R. H., Haber J. E. Meiotic recombination in yeast: alteration by multiple heterozygosities. Science. 1987 Sep 18;237(4821):1459–1465. doi: 10.1126/science.2820060. [DOI] [PubMed] [Google Scholar]
  4. Burr B., Burr F. A., St John T. P., Thomas M., Davis R. W. Zein storage protein gene family of maize. An assessment of heterogeneity with cloned messenger RNA sequences. J Mol Biol. 1982 Jan 5;154(1):33–49. doi: 10.1016/0022-2836(82)90415-6. [DOI] [PubMed] [Google Scholar]
  5. Chaudhuri S., Messing J. RFLP mapping of the maize dzr1 locus, which regulates methionine-rich 10 kDa zein accumulation. Mol Gen Genet. 1995 Mar 20;246(6):707–715. doi: 10.1007/BF00290716. [DOI] [PubMed] [Google Scholar]
  6. Colot V., Maloisel L., Rossignol J. L. Interchromosomal transfer of epigenetic states in Ascobolus: transfer of DNA methylation is mechanistically related to homologous recombination. Cell. 1996 Sep 20;86(6):855–864. doi: 10.1016/s0092-8674(00)80161-0. [DOI] [PubMed] [Google Scholar]
  7. Das O. P., Levi-Minzi S., Koury M., Benner M., Messing J. A somatic gene rearrangement contributing to genetic diversity in maize. Proc Natl Acad Sci U S A. 1990 Oct;87(20):7809–7813. doi: 10.1073/pnas.87.20.7809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Das O. P., Ward K., Ray S., Messing J. Sequence variation between alleles reveals two types of copy correction at the 27-kDa zein locus of maize. Genomics. 1991 Dec;11(4):849–856. doi: 10.1016/0888-7543(91)90007-2. [DOI] [PubMed] [Google Scholar]
  9. Dooner H. K. Genetic Fine Structure of the BRONZE Locus in Maize. Genetics. 1986 Aug;113(4):1021–1036. doi: 10.1093/genetics/113.4.1021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dooner H. K., Martínez-Férez I. M. Recombination occurs uniformly within the bronze gene, a meiotic recombination hotspot in the maize genome. Plant Cell. 1997 Sep;9(9):1633–1646. doi: 10.1105/tpc.9.9.1633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Eggleston W. B., Alleman M., Kermicle J. L. Molecular organization and germinal instability of R-stippled maize. Genetics. 1995 Sep;141(1):347–360. doi: 10.1093/genetics/141.1.347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Fink G. R., Styles C. A. Gene conversion of deletions in the his4 region of yeast. Genetics. 1974 Jun;77(2):231–244. doi: 10.1093/genetics/77.2.231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Geetha K. B., Lending C. R., Lopes M. A., Wallace J. C., Larkins B. A. opaque-2 modifiers increase gamma-zein synthesis and alter its spatial distribution in maize endosperm. Plant Cell. 1991 Nov;3(11):1207–1219. doi: 10.1105/tpc.3.11.1207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hu W., Das O. P., Messing J. Zeon-1, a member of a new maize retrotransposon family. Mol Gen Genet. 1995 Aug 30;248(4):471–480. doi: 10.1007/BF02191647. [DOI] [PubMed] [Google Scholar]
  15. Judd S. R., Petes T. D. Physical lengths of meiotic and mitotic gene conversion tracts in Saccharomyces cerevisiae. Genetics. 1988 Mar;118(3):401–410. doi: 10.1093/genetics/118.3.401. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Klein H. L., Petes T. D. Intrachromosomal gene conversion in yeast. Nature. 1981 Jan 15;289(5794):144–148. doi: 10.1038/289144a0. [DOI] [PubMed] [Google Scholar]
  17. Kostriken R., Strathern J. N., Klar A. J., Hicks J. B., Heffron F. A site-specific endonuclease essential for mating-type switching in Saccharomyces cerevisiae. Cell. 1983 Nov;35(1):167–174. doi: 10.1016/0092-8674(83)90219-2. [DOI] [PubMed] [Google Scholar]
  18. Llaca V., Messing J. Amplicons of maize zein genes are conserved within genic but expanded and constricted in intergenic regions. Plant J. 1998 Jul;15(2):211–220. doi: 10.1046/j.1365-313x.1998.00200.x. [DOI] [PubMed] [Google Scholar]
  19. McKnight G. L., Cardillo T. S., Sherman F. An extensive deletion causing overproduction of yeast iso-2-cytochrome c. Cell. 1981 Aug;25(2):409–419. doi: 10.1016/0092-8674(81)90059-3. [DOI] [PubMed] [Google Scholar]
  20. Meselson M. S., Radding C. M. A general model for genetic recombination. Proc Natl Acad Sci U S A. 1975 Jan;72(1):358–361. doi: 10.1073/pnas.72.1.358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Nag D. K., White M. A., Petes T. D. Palindromic sequences in heteroduplex DNA inhibit mismatch repair in yeast. Nature. 1989 Jul 27;340(6231):318–320. doi: 10.1038/340318a0. [DOI] [PubMed] [Google Scholar]
  22. Pays E., Van Assel S., Laurent M., Darville M., Vervoort T., Van Meirvenne N., Steinert M. Gene conversion as a mechanism for antigenic variation in trypanosomes. Cell. 1983 Sep;34(2):371–381. doi: 10.1016/0092-8674(83)90371-9. [DOI] [PubMed] [Google Scholar]
  23. Pukkila P. J., Stephens M. D., Binninger D. M., Errede B. Frequency and directionality of gene conversion events involving the CYC7-H3 mutation in Saccharomyces cerevisiae. Genetics. 1986 Oct;114(2):347–361. doi: 10.1093/genetics/114.2.347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Reynaud C. A., Anquez V., Grimal H., Weill J. C. A hyperconversion mechanism generates the chicken light chain preimmune repertoire. Cell. 1987 Feb 13;48(3):379–388. doi: 10.1016/0092-8674(87)90189-9. [DOI] [PubMed] [Google Scholar]
  25. Schwacha A., Kleckner N. Identification of double Holliday junctions as intermediates in meiotic recombination. Cell. 1995 Dec 1;83(5):783–791. doi: 10.1016/0092-8674(95)90191-4. [DOI] [PubMed] [Google Scholar]
  26. Strathern J. N., Shafer B. K., McGill C. B. DNA synthesis errors associated with double-strand-break repair. Genetics. 1995 Jul;140(3):965–972. doi: 10.1093/genetics/140.3.965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Sugawara N., Haber J. E. Characterization of double-strand break-induced recombination: homology requirements and single-stranded DNA formation. Mol Cell Biol. 1992 Feb;12(2):563–575. doi: 10.1128/mcb.12.2.563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Sun H., Treco D., Schultes N. P., Szostak J. W. Double-strand breaks at an initiation site for meiotic gene conversion. Nature. 1989 Mar 2;338(6210):87–90. doi: 10.1038/338087a0. [DOI] [PubMed] [Google Scholar]
  29. Sun H., Treco D., Szostak J. W. Extensive 3'-overhanging, single-stranded DNA associated with the meiosis-specific double-strand breaks at the ARG4 recombination initiation site. Cell. 1991 Mar 22;64(6):1155–1161. doi: 10.1016/0092-8674(91)90270-9. [DOI] [PubMed] [Google Scholar]
  30. Szostak J. W., Orr-Weaver T. L., Rothstein R. J., Stahl F. W. The double-strand-break repair model for recombination. Cell. 1983 May;33(1):25–35. doi: 10.1016/0092-8674(83)90331-8. [DOI] [PubMed] [Google Scholar]
  31. Thaler D. S., Stahl F. W. DNA double-chain breaks in recombination of phage lambda and of yeast. Annu Rev Genet. 1988;22:169–197. doi: 10.1146/annurev.ge.22.120188.001125. [DOI] [PubMed] [Google Scholar]
  32. Thuriaux P. Is recombination confined to structural genes on the eukaryotic genome? Nature. 1977 Aug 4;268(5619):460–462. doi: 10.1038/268460a0. [DOI] [PubMed] [Google Scholar]
  33. Timmermans M. C., Das O. P., Bradeen J. M., Messing J. Region-specific cis- and trans-acting factors contribute to genetic variability in meiotic recombination in maize. Genetics. 1997 Jul;146(3):1101–1113. doi: 10.1093/genetics/146.3.1101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Timmermans M. C., Das O. P., Messing J. Characterization of a meiotic crossover in maize identified by a restriction fragment length polymorphism-based method. Genetics. 1996 Aug;143(4):1771–1783. doi: 10.1093/genetics/143.4.1771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Yue X. N., Sakaguchi B., Eickbush T. H. Gene conversions can generate sequence variants in the late chorion multigene families of Bombyx mori. Genetics. 1988 Sep;120(1):221–231. doi: 10.1093/genetics/120.1.221. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES