Genomic sequencing.
Journal: 1984/May - Proceedings of the National Academy of Sciences of the United States of America
ISSN: 0027-8424
PUBMED: 6326095
Abstract:
Unique DNA sequences can be determined directly from mouse genomic DNA. A denaturing gel separates by size mixtures of unlabeled DNA fragments from complete restriction and partial chemical cleavages of the entire genome. These lanes of DNA are transferred and UV-crosslinked to nylon membranes. Hybridization with a short 32P-labeled single-stranded probe produces the image of a DNA sequence "ladder" extending from the 3' or 5' end of one restriction site in the genome. Numerous different sequences can be obtained from a single membrane by reprobing. Each band in these sequences represents 3 fg of DNA complementary to the probe. Sequence data from mouse immunoglobulin heavy chain genes from several cell types are presented. The genomic sequencing procedures are applicable to the analysis of genetic polymorphisms, DNA methylation at deoxycytidines, and nucleic acid-protein interactions at single nucleotide resolution.
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Proc Natl Acad Sci U S A 81(7): 1991-1995

Genomic sequencing.

Abstract

Unique DNA sequences can be determined directly from mouse genomic DNA. A denaturing gel separates by size mixtures of unlabeled DNA fragments from complete restriction and partial chemical cleavages of the entire genome. These lanes of DNA are transferred and UV-crosslinked to nylon membranes. Hybridization with a short 32P-labeled single-stranded probe produces the image of a DNA sequence "ladder" extending from the 3' or 5' end of one restriction site in the genome. Numerous different sequences can be obtained from a single membrane by reprobing. Each band in these sequences represents 3 fg of DNA complementary to the probe. Sequence data from mouse immunoglobulin heavy chain genes from several cell types are presented. The genomic sequencing procedures are applicable to the analysis of genetic polymorphisms, DNA methylation at deoxycytidines, and nucleic acid-protein interactions at single nucleotide resolution.

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Selected References

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  • Doerfler W. DNA methylation and gene activity. Annu Rev Biochem. 1983;52:93–124. [PubMed] [Google Scholar]
  • Bird AP, Southern EM. Use of restriction enzymes to study eukaryotic DNA methylation: I. The methylation pattern in ribosomal DNA from Xenopus laevis. J Mol Biol. 1978 Jan 5;118(1):27–47. [PubMed] [Google Scholar]
  • Busslinger M, deBoer E, Wright S, Grosveld FG, Flavell RA. The sequence GGCmCGG is resistant to MspI cleavage. Nucleic Acids Res. 1983 Jun 11;11(11):3559–3569.[PMC free article] [PubMed] [Google Scholar]
  • Keshet E, Cedar H. Effect of CpG methylation on Msp I. Nucleic Acids Res. 1983 Jun 11;11(11):3571–3580.[PMC free article] [PubMed] [Google Scholar]
  • Simon D, Stuhlmann H, Jähner D, Wagner H, Werner E, Jaenisch R. Retrovirus genomes methylated by mammalian but not bacterial methylase are non-infectious. Nature. 1983 Jul 21;304(5923):275–277. [PubMed] [Google Scholar]
  • Busslinger M, Hurst J, Flavell RA. DNA methylation and the regulation of globin gene expression. Cell. 1983 Aug;34(1):197–206. [PubMed] [Google Scholar]
  • Ohmori H, Tomizawa JI, Maxam AM. Detection of 5-methylcytosine in DNA sequences. Nucleic Acids Res. 1978 May;5(5):1479–1485.[PMC free article] [PubMed] [Google Scholar]
  • Miller JR, Cartwright EM, Brownlee GG, Fedoroff NV, Brown DD. The nucleotide sequence of oocyte 5S DNA in Xenopus laevis. II. The GC-rich region. Cell. 1978 Apr;13(4):717–725. [PubMed] [Google Scholar]
  • Maxam AM, Gilbert W. Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol. 1980;65(1):499–560. [PubMed] [Google Scholar]
  • Rubin CM, Schmid CW. Pyrimidine-specific chemical reactions useful for DNA sequencing. Nucleic Acids Res. 1980 Oct 24;8(20):4613–4619.[PMC free article] [PubMed] [Google Scholar]
  • Alwine JC, Kemp DJ, Stark GR. Method for detection of specific RNAs in agarose gels by transfer to diazobenzyloxymethyl-paper and hybridization with DNA probes. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5350–5354.[PMC free article] [PubMed] [Google Scholar]
  • Seed B. Diazotizable arylamine cellulose papers for the coupling and hybridization of nucleic acids. Nucleic Acids Res. 1982 Mar 11;10(5):1799–1810.[PMC free article] [PubMed] [Google Scholar]
  • Southern EM. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. [PubMed] [Google Scholar]
  • Arnheim N, Southern EM. Heterogeneity of the ribosomal genes in mice and men. Cell. 1977 Jun;11(2):363–370. [PubMed] [Google Scholar]
  • Reiser J, Renart J, Stark GR. Transfer of small DNA fragments from polyacrylamide gels to diazobenzyloxymethyl-paper and detection by hybridization with DNA probes. Biochem Biophys Res Commun. 1978 Dec 14;85(3):1104–1112. [PubMed] [Google Scholar]
  • Kutateladze TV, Axelrod VD, Gorbulev VG, Belzhelarskaya SN, Vartikyan RM. New procedure of high-voltage electrophoresis in polyacrylamide gel and its application to the sequencing of nucleic acids. Anal Biochem. 1979 Nov 15;100(1):129–135. [PubMed] [Google Scholar]
  • Bittner M, Kupferer P, Morris CF. Electrophoretic transfer of proteins and nucleic acids from slab gels to diazobenzyloxymethyl cellulose or nitrocellulose sheets. Anal Biochem. 1980 Mar 1;102(2):459–471. [PubMed] [Google Scholar]
  • Stellwag EJ, Dahlberg AE. Electrophoretic transfer of DNA, RNA and protein onto diazobenzyloxymethyl (DBM) - paper. Nucleic Acids Res. 1980 Jan 25;8(2):299–317.[PMC free article] [PubMed] [Google Scholar]
  • Smith GE, Summers MD. The bidirectional transfer of DNA and RNA to nitrocellulose or diazobenzyloxymethyl-paper. Anal Biochem. 1980 Nov 15;109(1):123–129. [PubMed] [Google Scholar]
  • Levy A, Frei E, Noll M. Efficient transfer of highly resolved small DNA fragments from polyacrylamide gels to DBM paper. Gene. 1980 Nov;11(3-4):283–290. [PubMed] [Google Scholar]
  • Thomas PS. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci U S A. 1980 Sep;77(9):5201–5205.[PMC free article] [PubMed] [Google Scholar]
  • Messing J. New M13 vectors for cloning. Methods Enzymol. 1983;101:20–78. [PubMed] [Google Scholar]
  • Zinn K, DiMaio D, Maniatis T. Identification of two distinct regulatory regions adjacent to the human beta-interferon gene. Cell. 1983 Oct;34(3):865–879. [PubMed] [Google Scholar]
  • Swanstrom R, Shank PR. X-Ray Intensifying Screens Greatly Enhance the Detection by Autoradiography of the Radioactive Isotopes 32P and 125I. Anal Biochem. 1978 May;86(1):184–192. [PubMed] [Google Scholar]
  • Tonegawa S. Somatic generation of antibody diversity. Nature. 1983 Apr 14;302(5909):575–581. [PubMed] [Google Scholar]
  • Wysocki LJ, Sato VL. "Panning" for lymphocytes: a method for cell selection. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2844–2848.[PMC free article] [PubMed] [Google Scholar]
  • Ralph P, Nakoinz I. Lipopolysaccharides inhibit lymphosarcoma cells of bone marrow orgin. Nature. 1974 May 3;249(452):49–51. [PubMed] [Google Scholar]
  • Siden EJ, Baltimore D, Clark D, Rosenberg NE. Immunoglobulin synthesis by lymphoid cells transformed in vitro by Abelson murine leukemia virus. Cell. 1979 Feb;16(2):389–396. [PubMed] [Google Scholar]
  • Kawakami T, Takahashi N, Honjo T. Complete nucleotide sequence of mouse immunoglobulin mu gene and comparison with other immunoglobulin heavy chain genes. Nucleic Acids Res. 1980 Sep 11;8(17):3933–3945.[PMC free article] [PubMed] [Google Scholar]
  • Auffray C, Rougeon F. Nucleotide sequence of a cloned cDNA corresponding to secreted mu chain of mouse immunoglobulin. Gene. 1980 Dec;12(1-2):77–86. [PubMed] [Google Scholar]
  • Goldberg GI, Vanin EF, Zrolka AM, Blattner FR. Sequence of the gene for the constant region of the mu chain of Balb/c mouse immunoglobulin. Gene. 1981 Oct;15(1):33–42. [PubMed] [Google Scholar]
  • Yagi M, Koshland ME. Expression of the J chain gene during B cell differentiation is inversely correlated with DNA methylation. Proc Natl Acad Sci U S A. 1981 Aug;78(8):4907–4911.[PMC free article] [PubMed] [Google Scholar]
  • Rogers J, Wall R. Immunoglobulin heavy chain genes: demethylation accompanies class switching. Proc Natl Acad Sci U S A. 1981 Dec;78(12):7497–7501.[PMC free article] [PubMed] [Google Scholar]
  • Storb U, Arp B. Methylation patterns of immunoglobulin genes in lymphoid cells: correlation of expression and differentiation with undermethylation. Proc Natl Acad Sci U S A. 1983 Nov;80(21):6642–6646.[PMC free article] [PubMed] [Google Scholar]
  • Leary JJ, Brigati DJ, Ward DC. Rapid and sensitive colorimetric method for visualizing biotin-labeled DNA probes hybridized to DNA or RNA immobilized on nitrocellulose: Bio-blots. Proc Natl Acad Sci U S A. 1983 Jul;80(13):4045–4049.[PMC free article] [PubMed] [Google Scholar]
Abstract
Unique DNA sequences can be determined directly from mouse genomic DNA. A denaturing gel separates by size mixtures of unlabeled DNA fragments from complete restriction and partial chemical cleavages of the entire genome. These lanes of DNA are transferred and UV-crosslinked to nylon membranes. Hybridization with a short 32P-labeled single-stranded probe produces the image of a DNA sequence "ladder" extending from the 3' or 5' end of one restriction site in the genome. Numerous different sequences can be obtained from a single membrane by reprobing. Each band in these sequences represents 3 fg of DNA complementary to the probe. Sequence data from mouse immunoglobulin heavy chain genes from several cell types are presented. The genomic sequencing procedures are applicable to the analysis of genetic polymorphisms, DNA methylation at deoxycytidines, and nucleic acid-protein interactions at single nucleotide resolution.
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