Ex parte RASMUSSEN et al. - Page 10


                  Appeal No.  1998-1719                                                                                      
                  Application No.  08/442,603                                                                                
                  GRIMES,  Administrative Patent Judge, concurring.                                                          
                         Although I agree that the obviousness rejection should be reversed, I                               
                  respectfully disagree with the majority’s analysis of the prima facie case.  The                           
                  majority concludes that the prima facie case fails because the examiner “fails to                          
                  identify a teaching, and we find no such teaching of record, that would suggest to a                       
                  person of ordinary skill in the art to modify the translation start site of the                            
                  glucocerebrosidase gene as was done in appellants’ pGB20 construct.”  However,                             
                  Appellants have admitted that the modification they made to the pGB20 translation                          
                  start site was known in the art to optimize expression in mammalian cells.                                 
                         The modification of the glucocerebrosidase translation start site in pGB20 is                       
                  explained in Appellants’ specification as follows:                                                         
                         To optimize expression of GCR in mammalian cells, we further                                        
                         modified the GCR.D21 BglII cassette containing the gcr gene.  In                                    
                         general, with reference to Fig. 6, the modifications were made using                                
                         oligonucleotide directed mutagenesis . . . to alter the nucleotide                                  
                         sequence near the GCR translation start to match the consensus                                      
                         sequence (CCACCATGG) for optimal translation in mammalian cells                                     
                         (as described by Kozak, 1986, 44 Cell 283-292).                                                     
                  Page 18.  This passage is an admission that a consensus translation start site had                         
                  been disclosed in the prior art and that such a translation start site was known to                        
                  provide optimal translation in mammalian cells.                                                            
                         Information that an applicant admits is in the prior art “may be considered                         
                  ‘prior art’ for any purpose, including use as evidence of obviousness under                                
                  35 U.S.C. § 103.”  In re Nomiya, 509 F.2d 566, 570-71, 184 USPQ 607, 611                                   
                  (CCPA 1975).  In addition, when considering obviousness, “the prior art as a whole                         
                  must be considered.  The teachings are to be viewed as they would have been                                

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