BIOL10005 Lecture Notes - Lecture 4: Sickle-Cell Disease, Hbb, Sister Chromatids

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Genetic consequences of meiosis, segregation of alleles. At anaphase 2, sister chromatids separate -> duplicates: independent assortment of chromosomes, crossing over and recombination of alleles. Pare(cid:374)ts" phe(cid:374)otypes are ho(cid:373)ozygous red a(cid:374)d ho(cid:373)ozygous white, f1 heterozygote phenotype is pink. > depends on how much enzyme that produces red pigment is present; crcr leads to red, Cwcw leads to white, crcw leads to incomplete dominance, pink. The full effect of both alleles can be seen as the phenotype of the heterozygote e. g. ) Alleles: normal -> hba, sickle cell (abnormal beta globin) -> hbs. 1:2:1: extensions to mendel: (other factors that alter gene expressions, multiple alleles. When more than two alternative are possible for a gene locus (one gene locus may have possibility to choose 2 from 4 alleles) e. g. ) Copy of an inherited condition but results from an environmental factor (environment modifies the phenotype to mimic the effect of a specific genotype) e. g. )

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