Ex Parte Coleman et al - Page 12


                  Appeal No.  2005-1422                                                           Page 12                   
                  Application No.  09/997,522                                                                               
                                They are related to other T7Gs by their seven hydrophobic                                   
                         domains which span the plasma membrane and form a bundle of                                        
                         antiparallel α helices.                                                                            
                  On reflection, appellants’ specification does not identify, or disclose a naturally                       
                  occurring human variant of the polynucleotide sequence of SEQ ID NO: 1.  At                               
                  best, appellants’ specification suggests that the claimed variant may encode a                            
                  member of the large family of T7G receptors, one of which is encoded by the                               
                  polynucleotide of SEQ ID NO: 1.                                                                           
                         Against this backdrop, we note that the examiner finds (Supplemental                               
                  Answer, page 7),                                                                                          
                         the scope of the claims includes numerous structural variants, and                                 
                         the genus is highly variant because a significant number of                                        
                         structural differences between genus members is permitted. The                                     
                         specification and claims do not provide any guidance as to what                                    
                         changes are made to SEQ ID NO:1 … to be considered a naturally                                     
                         occurring human variant….  Structural features that could                                          
                         distinguish compounds in the genus from others in the                                              
                         polynucleotide … class are missing from the disclosure.  No                                        
                         common structural attributes identify the members of the genus.                                    
                         The general knowledge and level of skill in the art do not                                         
                         supplement the omitted description because specific, not general,                                  
                         guidance is what is needed. Since the disclosure fails to describe                                 
                         the common attributes or characteristics that identify members of                                  
                         the genus, and because the genus is highly variant, SEQ ID NO: 1                                   
                         … alone … [is] insufficient to describe the genus.                                                 
                         In response, appellants assert (Brief, page 37), “[v]ariants of SEQ ID NO:                         
                  1 and SEQ ID NO:2 are described in the specification at, for example, page 4,                             
                  lines 30-32; page 5, lines 22-25; page 5, line 30 to page 6, line 11; page 7, lines                       
                  17-23; and page 8, lines 14-29.”  With regard to variants of a polynucleotide                             
                  sequence, as discussed above, the cited portions of the specification do not refer                        
                  to “naturally occurring human variants,” but instead address “recombinant                                 
                  nucleotide variants.”  In addition, as defined in appellants’ specification at page 7,                    





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