
Originally Posted by
Moonbeam
Off the top of my head, so without a reference: There are processes which cause genes to be repeated within the genome (mistakes during copying, genes which are transported within the genome, etc.) which cause additional copies of genes to be present. These copies can be worked on by mutations without detriment to the organisms carrying them; and when (rarely) a beneficial mutation is achieved, it can be propagated.
For example, the molecule hemoglobin: there are several copies of the genes that code for the proteins that make up hemoglobin. Some of these are used at different stages of development (a fetus has a different type of hemoglobin than an adult), some are found in people whom under certain circumstances, cause a disease, but under other circumstances protect the individual from malaria (hemoglobin S, the cause of sickle cell disease), and others which are totally non-functional genes that do not code for a protein at all, but are still recognizable as mutated copies of the hemoglobin gene. There are many other examples of these repeated and copied genes, available for "development" by evolution.
Does that answer the question?
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