The genetic information of human beings is contained in DNA molecules, which are structured as a double helix. These contain the information for cells to replicate, and also the ability to join with another set of DNA to produce another human being. Given that the genetic coding is in the form of a double helix, and each human has one double-helix structure, is each double helix reduced to a single strand prior to joining with the mate's single strand, or are both double helixes joined, then "sorted out" upon conception and subsequent development within the embryo?
The nature of dominant and recessive genes had me wondering about when the individual strands are combined into just two strands to form the double helix that the new person has. Since the male and female each contribute a double helix, but the new person still only has a double helix (as opposed to a quadruple helix), the combination has to occur at some point. Whatchya got?
The nature of dominant and recessive genes had me wondering about when the individual strands are combined into just two strands to form the double helix that the new person has. Since the male and female each contribute a double helix, but the new person still only has a double helix (as opposed to a quadruple helix), the combination has to occur at some point. Whatchya got?