50 likes | 214 Views
Chromosomes & Inheritance. The chromosomal basis for inheritance was described in 1902 independently by a group of scientists. It basically states that genes have specific loci on chromosomes and that during mitosis and meiosis the segregate and undergo independent assortment.
E N D
Chromosomes & Inheritance • The chromosomal basis for inheritance was described in 1902 independently by a group of scientists. It basically states that genes have specific loci on chromosomes and that during mitosis and meiosis the segregate and undergo independent assortment. • Thomas Hunt Morgan proved theory with the use of fruit flies (Drosophila melanogaster).
Mutant vsWildtype • Because of their fast reproductive cycle and their ease of use, Drosophila melanogaster quickly became a model organism for the study genetics. • most common trait is the wild type and less common trait the mutant type • traits named by the mutant type (human genes named by the wild type) • white eyes w; red eyes w+ • determined red is dominant with white being expressed more often in males (sex linked recessive)
genes on located on the same chromosome are linked • demonstrated with body color (gray & black (b & b+)) & wing shape (normal & vestigial (vg & vg+) • F1 all gray with normal wings • test cross ( F1 with true breeding recessive (b b+ vg vg+ x b+ b+ vg+ vg+) • if genes are located on separate genes the recombinants should be numerically equal for all traits • results are as follows: • cross yielded 965 gray-normal, 944 black vestigial, 206 gray-vestigial, & 185 black-normal • since 2 phenotypes are mostly present the genes are linked • the small percentage of mutants are due to crossing over • the greater the percentage of new recombinants the greater the distance of the genes on the same chromosome
Chromosomal basis of inheritance • Humans & many animals • X & Y • the presence of the Y determines male • contains the region SRY (sex-determining region of Y) • although the chromosomes are different in most aspects, there is a small homologous region that allows the 2 chromosomes to act as homologues during meiosis • penetrance of sex linked disorders from a female carrier • 50% of males (fragile-x, Duchenne Muscular Dystrophy, hemophelia) • 0% females unless the father has the disease, then 50% • random X-inactivation (lyonization) causes the creation of barr bodies • inactivation with methyl groups • condensed chromosome • reactivated when an ova is formed
Other Sex Determining Systems • X-O system (grasshopper) • XX vs X • XX female, X male • Z-W System (chicken) • ZW female, ZZ male • Haploid/diploid system (bees) • diploid - female, haploid - male