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Physical mapping of complex genomes

Patent 5219726 Issued on June 15, 1993. Estimated Expiration Date: Icon_subject June 15, 2010. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Vectors for in vitro production of RNA copies of either strand of a cloned DNA sequence Patent #: 4766072
Issued on: 08/23/1988
Inventor: Jendrisak ,   et al.

Inventor

Application

No. 360254 filed on 06/02/1989

US Classes:

435/6, Involving nucleic acid435/252.3, Transformants (e.g., recombinant DNA or vector or foreign or exogenous gene containing, fused bacteria, etc.)436/94, Saccharide (e.g., DNA, etc.)436/501BIOSPECIFIC LIGAND BINDING ASSAY

Examiners

Primary: Yarbrough, Amelia B.
Assistant: Zitomer, Stephanie W.

Attorney, Agent or Firm

International Classes

C12Q 001/68
C12N 001/20
G01N 033/566
G01N 033/48

Abstract

Method for simultaneous identification of overlapping cosmid clones among multiple cosmid clones and the use of the method for mapping complex genomes are provided. A library of cosmid clones that contains the DNA to be mapped is constructed and arranged in a manner such that individual clones can be identified and replicas of the arranged clones prepared.In preferred embodiments, the clones are arranged in a two dimensional matrix. In such embodiments, the cosmid clones in a row are pooled, mixed probes complementary to the ends of the DNA inserts int he pooled clones are synthesized, hybridized to a first replica of the library. Hybridizing clones, which include the pooled row, are identified. A second portion of clones is prepared by pooling cosmid clones that correspond to a column in the matrix. The second pool thereby includes one clone from the first portion pooled clones. This common clone is located on the replica at the intersection of the column and row. Mixed probes complementary to the ends of the DNA inserts in the second pooled portion of clones are prepared and hybridized to a second replica of the library. The hybridization pattern on the first and second replicas of the library are compared and cross-hybridizing clones, other than the clones in the pooled column and row, that hybridize to identical clones in the first and second replicas are identified. These clones necessarily include DNA inserts that overlap with the DNA insert int he common clone located at the intersection of the pooled row and pooled column.The DNA in the entire library may be mapped by pooling the clones in each of the rows and columns of the matrix, preparing mixed end-specific probes and hybridizing the probes from each row or column to a replica of the library. Since all clones in the library are located at the intersection of a column and a row, the overlapping clones for all clones in the library may be identified and a physical map constructed.In other preferred embodiments, the cosmid clones are arranged in a three dimensional matrix, pooled and compared in threes according to intersecting planes of the three dimensional matrix. Arrangements corresponding to geometries of higher dimensions may also be prepared and used to simultaneously identify overlapping clones in highly complex libraries with relatively few hybridization reactions.

Other References

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  • Coulson et al., Proc. Natl. Acad. Sci. USA 83, 7821
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  • Bates et al., Gene 26, 137 (1983)
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  • Poustka et al., Cold Springs Harbor Symposia on Quantitative Biology LI, 131 (1986)
  • Evans et al., Immunogenetics 28, 365 (1988
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