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Sequence, organization and expression of the core histone genes ofAspergillus nidulans

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Summary

The core histone gene family ofAspergillus nidulans was characterized. The H2A, H2B and H3 genes are unique in theA. nidulans genome. In contrast there are two H4 genes, H4.1 and H4.2. As previously reported for the H2A gene (May and Morris 1987) introns also interrupt the other core histone genes. The H2B gene, like the H2A gene, is interrupted by three introns, the H3 and H4.1 gene are each interrupted by two introns and the H4.2 gene contains one intron. The position of the single intron in H4.2 is the same as that the first intron of the H4.1 gene. The H2A and H2B genes are arranged as a gene pair separated by approximately 600 by and are divergently transcribed. The H3 and H4.1 genes are similarly arranged and are separated by approximately 800 bp. The H4.2 gene is not closely linked to either the H2A-H2B or H3-H4.1 gene pairs. Using pulse field gel electrophoresis an electrophoretic karyotype was established forA. nidulans. This karyotype was used to assign the H3–H4.1 gene pair and the H4.2 gene to linkage group VIII and the H2A–H2B gene pair to either linkage group III or VI. The abundance of each of the histone messenger RNAs was determined to be cell cycle regulated but the abundance of the H4.2 mRNA appears to be regulated differently from the others.

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References

  • Benton WD, Davis RW (1977) Screening λgt recombinant clones by hybridization to single plaques in situ. Science 196:180–182

    Google Scholar 

  • Boylan MT, Mirabito PM, Willett CE, Zimmerman CR, Timberlake WE (1987) Isolation and physical characterization of three essential conidiation genes fromA. nidulans. Mol Cell Biol 7:3113–3118

    Google Scholar 

  • Brody H, Carbon J (1989) Electrophoretic karyotype ofAspergillus nidulans. Proc Natl Acad Sci USA 86:6260–6263

    Google Scholar 

  • Brush D, Dodgson JB, Choi O-R, Stevens PW, Engle JD (1985) Replacement variant histone genes contain intervening sequences. Mol Cell Biol 5:1307–1317

    Google Scholar 

  • Choe JD, Kolodrubetz D, Grunstein M (1982) The two yeast historic H2A genes encode similar protein subtypes. Proc Natl Acad Sci USA 79:1484–1487

    Google Scholar 

  • Choe J, Schuster T, Grunstein M (1985) Organization, primary structure and evolution of historic H2A and H2B genes of the fission yeastSchizosaccharomyces pombe. Mol Cell Biol 5:3261–3269

    Google Scholar 

  • Cove DJ (1966) The induction and repression of nitrate reductase in the fungusAspergillus nidulans. Biochim Biophys Acta 113:51–56

    Google Scholar 

  • Doonan JH, Morris NR (1989) ThebimG gene ofAspergillus nidulans, required for completion of anaphase, encodes a homolog of mammalian phosphoprotein phosphatase 1. Cell 57:987–996

    Google Scholar 

  • Farrel-Towt J, Sanders MM (1984) Noncoordiante histone synthesis in heatshockedDrosophila cells is regulated at multiple levels. Mol Cell Biol 4:2676–2685

    Google Scholar 

  • Feinberg AP, Vogelstein B (1983) A technique for radiolabelling DNA restriction fragments to high specific activity. Anal Biochem 132:6–13

    Google Scholar 

  • Felden RA, Sanders MM, Morris NR (1976) Presence of histories inAspergillus nidulans. J Cell Biol 68:430–439

    Google Scholar 

  • Fidel S, Doonan JH, Morris NR (1988)Aspergillus nodulans contains a single actin gene which has unique intron locations and encodes a gamma-actin. Gene 70:283–293

    Google Scholar 

  • Gibson TJ, Coulson AR, Sulston JE, Little PER (1987) Lorist2, a cosmid with transcriptional terminators insulating vector genes from interference by promoters within the insert: effect on DNA yield and cloned insert frequency. Gene 53:275–281

    Google Scholar 

  • Hereford L, Fahrner K, Woolford J Jr, Rosbash M, Kaback DB (1979) Isolation of yeast histone genes H2A and H2B. Cell 18:1261–1271

    Google Scholar 

  • Isenberg I (1979) Histories. Annu Rev Biochem 48:159–191

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning. A laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY

    Google Scholar 

  • Matsumoto S, Yanagida M (1985) Historic gene organization of the fission yeast: a common upstream sequence. EMBO J 4:3531–3538

    Google Scholar 

  • Maxson R, Cohn R, Kedes L, Mohun T (1983) Expression and organization of histone genes. Annu Rev Genet 17:239–277

    Google Scholar 

  • May GS, Morris NR (1987) The unique historic H2A gene ofAspergillus nidulans contains three introns. Gene 58:59–66

    Google Scholar 

  • May GS, Gambino J, Weatherbee JA, Morris NR (1985) Identification and functional analysis of β-tubulin genes by site specific integrative transformation inA. nidulans. J Cell Biol 101:712–719

    Google Scholar 

  • May GS, Tsang ML-S, Smith H, Fidel S, Morris NR (1987)Aspergillus nidulans β-tubulins are unusually divergent. Gene 55:231–243

    Google Scholar 

  • McGhee JD, Felsenfeld G (1980) Nucleosome structure. Annu Rev Biochem 49:1115–1156

    Google Scholar 

  • Messing J (1983) New M13 vectors for cloning. Methods Enzymol 101:20–78

    Google Scholar 

  • Morris NR (1976) Nucleosome structure inAspergillus nidulans. Cell 8:357–363

    Google Scholar 

  • Oakley BR, Rinehart JE, Mitchell BL, Oakley CE, Carmona C, Gray GL, May GS (1987) Cloning, mapping and molecular analysis of the pyrG gene (orotidine-5′-phosphate decarboxylase) gene ofAspergillus nidulans. Gene 61:385–399

    Google Scholar 

  • Orr WC, Timberlake WE (1982) Clustering of spore-specific genes inAspergillus nidulans. Proc Natl Acad Sci USA 79:5976–5980

    Google Scholar 

  • Osmani SA, May GS, Morris NR (1987) Regulation of the mRNA levels ofnimA, a gene required for the G2-M transition inAspergillus nidulans. J Cell Biol 104:1495–1504

    Google Scholar 

  • Osmani SA, Engle DB, Doonan JH, Morris NR (1988a) Spindle formation and chromatin condensation in cells blocked at interphase by mutation of a negative cell cycle control gene. Cell 52:241–251

    Google Scholar 

  • Osmani SA, Pu RT, Morris NR (1988b) Mitotic induction and maintenance by overexpression of a G2-specific gene that encodes a potential protein kinase. Cell 53:237–244

    Google Scholar 

  • Sanger FS, Nicklen S, Coulson AR (1977) DNA sequencing with chain terminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467

    Google Scholar 

  • Smith MM, Andresson OS (1983) DNA sequences of yeast H3 and H4 histone genes from two non-allelic gene sets encode identical H3 and H4 proteins. J Mol Biol 169:663–690

    Google Scholar 

  • Tabor S, Richardson CC (1987) DNA sequence analysis with a modified T7 DNA polymerase. Proc Natl Acad Sci USA 81:1470–1474

    Google Scholar 

  • Upshall A (1986) Genetic and molecular characterization ofargB + transformants ofA. nidulans. Curr Genet 10:593–599

    Google Scholar 

  • Vollmer SJ, Yanofsky C (1986) Efficient cloning of genes ofNeurospora crassa. Proc Natl Acad Sci USA 83:4869–4873

    Google Scholar 

  • Wahl GM, Lewis KA, Ruiz JC, Rothenberg B, Zhao J, Evans GA (1987) Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer. Proc Natl Acad Sci USA 84:2160–2164

    Google Scholar 

  • Wallis JW, Hereford L, Grunstein M (1980) Historic H2B genes of yeast encode two different proteins. Cell 22:799–805

    Google Scholar 

  • Wells D, Kedes L (1987) Unusual structure, evolutionary conservation of non-coding sequences and numerous pseudogenes characterize the human H3.3 histone multigene family. Nucleic Acids Res 15:2871–2889

    Google Scholar 

  • Woudt LP, Pastink A, Kempers-Veenstra AE, Jansen AEM, Mager WH, Planta RJ (1983) The genes coding for histone H3 and H4 inNeurospora crassa are unique and contain intervening sequences. Nucleic Acids Res 11:5347–5360

    Google Scholar 

  • Wu M, Allis CD, Richman R, Cook RG, Gorovsky MA (1986) An intervening sequence in an unusual histone H1 gene ofTetrahymena thermophila. Proc Natl Acad Sci USA 83:8674–8678

    Google Scholar 

  • Yelton MM, Hamer JE, Timberlake WE (1984) Transformation ofAspergillus nidulans by using atrpC plasmid. Proc Natl Acad Sci USA 81:1470–1474

    Google Scholar 

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Communicated by C.A. van den Hondel

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Ehinger, A., Denison, S.H. & May, G.S. Sequence, organization and expression of the core histone genes ofAspergillus nidulans . Mol Gen Genet 222, 416–424 (1990). https://doi.org/10.1007/BF00633848

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