The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 06, 1995

Filed:

Apr. 20, 1993
Applicant:
Inventors:

Michael G Murray, Madison, WI (US);

Jane H Cramer, Madison, WI (US);

Jeanne Romero-Severson, Mazomainie, WI (US);

David West, Prescott, WI (US);

Yu Ma, Madison, WI (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A01H / ;
U.S. Cl.
CPC ...
47 58 ; 47DI / ; 4351723 ; 4351721 ;
Abstract

A set of nucleic acid probes useful for tracking Maize Dwarf Mosaic Virus Resistance (MDMV), a polygenic trait, is provided. Chromosome segments are identified enabling isolation of the genes governing this trait. A general method for identifying probes useful for tracking and introgressing polygenic traits into elite genomes and identifying chromosome segments governing the traits is also provided. This method involves the analysis of RFLP polymorphisms between parent donor and recipient genotypes and observed phenotypic data using multiple regression by leaps and bounds ('leaps'), followed by standard multiple regression applied to the 'leaps' data. The 'leaps' data may be used to identify flanking markers, and epistasis may be determined by analysis of the multiple regression data. Kits comprising a subset of the most useful probes (those most closely linked to the trait of interest) are provided. The kits may also comprise flanking probes. Flanking probes used in combination with the most closely linked probes are useful in identifying situations in which donor DNA tends to move in clumps and recovering rare individuals in which traits of interest have separated from surrounding donor DNA, so that elite recipient DNA may be maximized.


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