Ex Parte Turner et al - Page 18


              Appeal No. 2004-1040                                                        Page 18                        
              Application No. 09/770,643                                                                                 

              Id., page 17.  Appellants argue that “the practical scientific value of expressed, spliced,                
              and polyadenylated mRNA sequences is readily apparent to those skilled in the relevant                     
              biological and biochemical arts.”  Id.  Finally, Appellants argue that “the present                        
              nucleotide sequence has a specific utility in mapping the claimed sequence to the                          
              corresponding human chromosome, specifically chromosome 2.”  Id.                                           
                     We are not persuaded by Appellants’ argument.  We find that the asserted uses                       
              of the claimed polynucleotides—as a component of a DNA chip for monitoring gene                            
              expression, as a marker for a given chromosomal locus, or for defining the exon splice-                    
              junctions of a gene—do not satisfy the utility requirement of § 101.  Such uses do not                     
              provide a specific benefit in currently available form.                                                    
                     For example, with regard to the asserted “DNA chip” utility, we accept for                          
              argument’s sake that a person skilled in the art could attach one of the claimed                           
              polynucleotides (or a part of it) to a solid substrate, in combination with other                          
              polynucleotides, to form a DNA chip, and that such a DNA chip could be used to                             
              monitor changes in expression of the corresponding gene.  However, the specification                       
              provides no guidance to allow a skilled artisan to use data relating to the expression of                  
              the gene comprising SEQ ID NO:1 in any practical way.  The specification provides no                       
              guidance regarding what the SEQ ID NO:1-specific information derived from a DNA chip                       
              would mean.                                                                                                
                     For example, assume that a fragment of SEQ ID NO:1 was attached to a DNA                            
              chip and the researcher observed that expression of the corresponding gene was                             
              increased when a cell was treated with a particular agent.  The specification provides no                  
              basis on which a skilled worker would be able to determine what, if anything, that result                  





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