The techniques behind the investigation of freeradical, somatic mutation, and DNA-protein deterioration theories are no longer adequate to further our knowledge significantly on the role of DNA-protein complexes in aging dysfunction. Clearly, only the preliminaries were accomplished by studies based on the hypotheses of DNA-protein interactions for aging. As we see it, we urgently need to address ourselves to one simple question at a time, specifically to age changes in the DNA-protein complex, a potential site of primary changes leading to aging dysfunction.