Chapter 7
Genetics 001 with Rayotto at George Mason University
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By: Daniel Pinto
Created: 2010-10-14
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Created: 2010-10-14
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Karyotype: complete set of chromosomes possessed by an individual. Chromosomal mutation - Grouped into three categories Chromosomal Arrangements: Alter the structure of chromosomes. Duplications: part of a chromosome has been doubled. Tandem duplication mean that the duplication is immediately adjacent to the original segment AB*CDEFG AB*CDEF EF G. Are the sources of new genes that may provide novel functions. Displaced Deletion: usually causes death. it may also occur pseudo Dominance : the dominance of a receive gene over a *missing dominant gene. Effects in meiosis: In heterozygouse the body would loop the extra slack of the DNA that doesnt mach, not including the suplicated section for replication. HOw do mutations affect genotype: more genes means more proteins , upsetting the balance of proteins. WHere do duplication come from? duplications arise from Unequal Crossing over. UNequal crossingover couses an extension of the DNA Aneupliody: number of individual Polyploidy: karyotypes have one or more (or less) complete sets of chromosomes. INVERSIONS: Crossing over within paracentric inversions ---> NO recombinant progeny is found in this case. Translocation: exchange between non-homologouse chromosomes. Not to be confused with crossing over. The effects on phenotypes of translocation : position effect; effects on miosis: Robisonian translocation Translocation in Evolution : Summary : Chromosomal Rearrangements: What is duplication? part of chromosome is doubled WHat is deletion? Part of chromosome lost What are the effects of meiosis? loop and loop out of the normal What is an inversion: pericentric and paracentric.--> effect in meiosis often lethal What is translocation? part of choromosome moved up
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About this note
By: Daniel Pinto
Created: 2010-10-14
File Size: 1 page(s)
Views: 1
Created: 2010-10-14
File Size: 1 page(s)
Views: 1
About StudyBlue
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