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. 1992 Nov;11(11):4037–4046. doi: 10.1002/j.1460-2075.1992.tb05497.x

Molecular cloning and characterization of iojap (ij), a pattern striping gene of maize.

C D Han 1, E H Coe Jr 1, R A Martienssen 1
PMCID: PMC556914  PMID: 1382980

Abstract

Iojap (ij) is a recessive striped mutant of maize affecting the development of plastids in a local and position-dependent manner on the leaves. The ij-affected plastids are transmitted to some of the progeny even when the function of the nuclear gene is restored. Developmental defects during embryogenesis and leaf proliferation are other phenotypic characteristics of ij. The extent of striping and the degree of developmental arrest in ij depend upon genetic background. To understand the diverse and unique phenotypic expression of ij, a transposon tagging experiment has been conducted using Robertson's Mutator (Mu). A new ij mutant was obtained from crosses of the reference allele of (ij-ref) to Mu lines. Subsequent genetic and molecular studies showed that the mutant carried a new ij allele (ij-mum1) from the Mu lines and contained a Mu1 element that cosegregated with the iojap phenotype. A 6.0 kb EcoRI genomic DNA fragment containing the Mu1 element was cloned. ij-ref is unstable, and revertants (Ij-Rev) have been obtained. Using the flanking DNA from the genomic clone as a probe, DNA polymorphisms were detected between ij-ref and these revertants. Further, transcripts were restored to the normal level in Ij-Rev seedlings. Comparison of genomic DNA clones from ij-ref, ij-mum1 and Ij indicated that the ij-ref allele contained 1.5 kb of additional DNA related to a transposable element, Ds. Germinal and somatic revertant alleles were derived by excision of this 1.5 kb element from ij-ref. The structure of the Ij gene and the DNA sequence of its transcribed region were determined. The Ij gene encodes a 24.8 kDa protein that showed no significant sequence similarity with proteins listed in databases.

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Selected References

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  1. Barkan A., Martienssen R. A. Inactivation of maize transposon Mu suppresses a mutant phenotype by activating an outward-reading promoter near the end of Mu1. Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3502–3506. doi: 10.1073/pnas.88.8.3502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barkan A., Miles D., Taylor W. C. Chloroplast gene expression in nuclear, photosynthetic mutants of maize. EMBO J. 1986 Jul;5(7):1421–1427. doi: 10.1002/j.1460-2075.1986.tb04378.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Buckner B., Kelson T. L., Robertson D. S. Cloning of the y1 Locus of Maize, a Gene Involved in the Biosynthesis of Carotenoids. Plant Cell. 1990 Sep;2(9):867–876. doi: 10.1105/tpc.2.9.867. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Church G. M., Gilbert W. Genomic sequencing. Proc Natl Acad Sci U S A. 1984 Apr;81(7):1991–1995. doi: 10.1073/pnas.81.7.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Coen E. S., Carpenter R., Martin C. Transposable elements generate novel spatial patterns of gene expression in Antirrhinum majus. Cell. 1986 Oct 24;47(2):285–296. doi: 10.1016/0092-8674(86)90451-4. [DOI] [PubMed] [Google Scholar]
  6. Döring H. P., Starlinger P. Barbara McClintock's controlling elements: now at the DNA level. Cell. 1984 Dec;39(2 Pt 1):253–259. doi: 10.1016/0092-8674(84)90002-3. [DOI] [PubMed] [Google Scholar]
  7. Fowler R. G., Peterson P. A. An altered state of a specific en regulatory element induced in a maize tiller. Genetics. 1978 Dec;90(4):761–782. doi: 10.1093/genetics/90.4.761. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gruissem W. Chloroplast gene expression: how plants turn their plastids on. Cell. 1989 Jan 27;56(2):161–170. doi: 10.1016/0092-8674(89)90889-1. [DOI] [PubMed] [Google Scholar]
  9. Jenkins B. Spatiotemporal isosensitivity fields in the human visual system. Perception. 1986;15(4):467–472. doi: 10.1068/p150467. [DOI] [PubMed] [Google Scholar]
  10. Kunze R., Starlinger P. The putative transposase of transposable element Ac from Zea mays L. interacts with subterminal sequences of Ac. EMBO J. 1989 Nov;8(11):3177–3185. doi: 10.1002/j.1460-2075.1989.tb08476.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Luehrsen K. R., Walbot V. Insertion of Mu1 elements in the first intron of the Adh1-S gene of maize results in novel RNA processing events. Plant Cell. 1990 Dec;2(12):1225–1238. doi: 10.1105/tpc.2.12.1225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Martienssen R. A., Barkan A., Freeling M., Taylor W. C. Molecular cloning of a maize gene involved in photosynthetic membrane organization that is regulated by Robertson's Mutator. EMBO J. 1989 Jun;8(6):1633–1639. doi: 10.1002/j.1460-2075.1989.tb03553.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Martienssen R., Barkan A., Taylor W. C., Freeling M. Somatically heritable switches in the DNA modification of Mu transposable elements monitored with a suppressible mutant in maize. Genes Dev. 1990 Mar;4(3):331–343. doi: 10.1101/gad.4.3.331. [DOI] [PubMed] [Google Scholar]
  14. McCarty D. R., Carson C. B., Stinard P. S., Robertson D. S. Molecular Analysis of viviparous-1: An Abscisic Acid-Insensitive Mutant of Maize. Plant Cell. 1989 May;1(5):523–532. doi: 10.1105/tpc.1.5.523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. McLaughlin M., Walbot V. Cloning of a mutable bz2 allele of maize by transposon tagging and differential hybridization. Genetics. 1987 Dec;117(4):771–776. doi: 10.1093/genetics/117.4.771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ortiz D. F., Strommer J. N. The Mu1 maize transposable element induces tissue-specific aberrant splicing and polyadenylation in two Adh1 mutants. Mol Cell Biol. 1990 May;10(5):2090–2095. doi: 10.1128/mcb.10.5.2090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Peterson P A. The Pale Green Mutable System in Maize. Genetics. 1960 Jan;45(1):115–133. doi: 10.1093/genetics/45.1.115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Pohlman R. F., Fedoroff N. V., Messing J. The nucleotide sequence of the maize controlling element Activator. Cell. 1984 Jun;37(2):635–643. doi: 10.1016/0092-8674(84)90395-7. [DOI] [PubMed] [Google Scholar]
  19. Rhoades M. M. Genic Induction of an Inherited Cytoplasmic Difference. Proc Natl Acad Sci U S A. 1943 Dec;29(11):327–329. doi: 10.1073/pnas.29.11.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Rowland L. J., Strommer J. N. Insertion of an unstable element in an intervening sequence of maize Adh1 affects transcription but not processing. Proc Natl Acad Sci U S A. 1985 May;82(9):2875–2879. doi: 10.1073/pnas.82.9.2875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Saedler H., Nevers P. Transposition in plants: a molecular model. EMBO J. 1985 Mar;4(3):585–590. doi: 10.1002/j.1460-2075.1985.tb03670.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Siemenroth A., Börner T., Metzger U. Biochemical studies on the iojap mutant of maize. Plant Physiol. 1980 Jun;65(6):1108–1110. doi: 10.1104/pp.65.6.1108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sutton W. D., Gerlach W. L., Peacock W. J., Schwartz D. Molecular analysis of ds controlling element mutations at the adh1 locus of maize. Science. 1984 Mar 23;223(4642):1265–1268. doi: 10.1126/science.223.4642.1265. [DOI] [PubMed] [Google Scholar]
  24. Taylor W. C., Barkan A., Martienssen R. A. Use of nuclear mutants in the analysis of chloroplast development. Dev Genet. 1987;8(5-6):305–320. doi: 10.1002/dvg.1020080503. [DOI] [PubMed] [Google Scholar]
  25. Towler D. A., Gordon J. I., Adams S. P., Glaser L. The biology and enzymology of eukaryotic protein acylation. Annu Rev Biochem. 1988;57:69–99. doi: 10.1146/annurev.bi.57.070188.000441. [DOI] [PubMed] [Google Scholar]
  26. Walbot V., Coe E. H. Nuclear gene iojap conditions a programmed change to ribosome-less plastids in Zea mays. Proc Natl Acad Sci U S A. 1979 Jun;76(6):2760–2764. doi: 10.1073/pnas.76.6.2760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Weck E., Courage U., Döring H. P., Fedoroff N., Starlinger P. Analysis of sh-m6233, a mutation induced by the transposable element Ds in the sucrose synthase gene of Zea mays. EMBO J. 1984 Aug;3(8):1713–1716. doi: 10.1002/j.1460-2075.1984.tb02036.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Wessler S. R., Baran G., Varagona M., Dellaporta S. L. Excision of Ds produces waxy proteins with a range of enzymatic activities. EMBO J. 1986 Oct;5(10):2427–2432. doi: 10.1002/j.1460-2075.1986.tb04517.x. [DOI] [PMC free article] [PubMed] [Google Scholar]

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