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Chapter 15 Chromosomes and Inheritance Dr. Joseph Silver
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we will study the following topics - sex linked diseases - human diseases - mutations
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there are 2 types of chromosomes - somatic chromosomes - sex chromosomes
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somatic chromosomes refer to the chromosomes that produce enzymes for almost every characteristic and function except for those genes on the sex chromosomes
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remember that you have chromosome pairs 1 from mom and one from dad they have genes for the same traits but the genes do not have to be identical although some of them can be identical
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this is true for females but it is NOT true for males in males the 22 somatic chromosomes are paired just like in females but the sex chromosomes are different
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the sex chromosomes have 2 functions - they contain genes for many functions - they determine the sex of an offspring
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females are referred to as XX males are referred to as XY the Y chromosome is much smaller than the X
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in a female the sex chromosomes XX have a copy of each gene on each X so females have 2 genes for each trait on the X
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males only have 1 X chromosome and the Y chromosome is much smaller than the X so males have many genes on the X which do not exist on the Y there are more than 1000 genes on the X which do not exist on the Y
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these 1000 genes do not exist as a pair in males these 1000 plus genes on the Y exist as a single gene and NOT as a pair
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sex-linked diseases refer to diseases caused by recessive genes which exist on the X but not on the Y
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if the gene on the X is normal a male will be normal but there are diseases caused by recessive genes if a male has the recessive gene for a disease on the X then the male will be sick because he only has 1 gene there is no second dominant gene to repress the recessive gene
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females in order to have a sex linked disease must have a recessive gene on both X chromosomes both parents had to give the child a recessive gene
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in females since they have 2 X chromosomes the normal dominant gene suppresses the expression of the recessive gene in order for a female to have a sex linked disease both parents must pass on the recessive gene
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in a male since they have many genes present as a single gene if they have a dominant gene = normal if they have 1 recessive gene for a disease = sick
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these are diseases which males have more than 10 times as often as females these are disease which mothers pass on to their sons dad gave you a Y – mom gave you an X these genes are only on the X these are sex-linked diseases
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there are many diseases which are found on the somatic chromosomes some are common others are rare some are caused by dominant genes some are caused by recessive genes
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But sex-linked diseases are caused by recessive genes on the chromosome if a male has 1 recessive gene for a disease they are sick a female must have 2 recessive genes to be sick
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cystic fibrosis – 1 enzyme sickle cell anemia – 1 enzyme hemophilia – 1 enzyme X-linked Huntington’s – dominant (45-50) Down’s syndrome – extra chromosome (21) color blindness – x linked (different kinds)
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Barr Bodies (methyl DNA inactivation) females = XX but in normal females one X is inactivated it condenses into a compact Barr Body
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which X is inactivated the one from mom or the one from dad takes place randomly at the time of inactivation the result is that in the embryo at the time of X inactivation some of mom’s X are inactivated and some of dad’s X are inactivated so females are mosaics (mosaicism)
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gene linkage genes which are close to each other on a chromosome are more likely to be passed on together and genes which are far from each other on a chromosome are less likely to be passed on together
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there are many kinds of errors point mutation ( + or -) base substitution (replace 1 base) addition (add a base) deletion (remove a base) inversions (invert a section) translocation (put a section into wrong place)
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all cells whether in a single celled prokaryote or a large multicellular eukaryote are exposed to substances called mutagens which cause errors in DNA known as mutations
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some mutations cause an error in one amino acid but some mutations cause the entire protein from that point on to be incorrect
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genomic imprinting phenotype depends on which parent passed on the gene probably hundreds of genes (know 60)
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