* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Chapter 10 Genetics: Mendel and Beyond
Human genetic variation wikipedia , lookup
Heritability of IQ wikipedia , lookup
Ridge (biology) wikipedia , lookup
Therapeutic gene modulation wikipedia , lookup
Polycomb Group Proteins and Cancer wikipedia , lookup
Public health genomics wikipedia , lookup
Site-specific recombinase technology wikipedia , lookup
Genome evolution wikipedia , lookup
Biology and consumer behaviour wikipedia , lookup
Nutriepigenomics wikipedia , lookup
Behavioural genetics wikipedia , lookup
Neocentromere wikipedia , lookup
Polymorphism (biology) wikipedia , lookup
Pharmacogenomics wikipedia , lookup
Skewed X-inactivation wikipedia , lookup
Population genetics wikipedia , lookup
Y chromosome wikipedia , lookup
Gene expression profiling wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Epigenetics of human development wikipedia , lookup
Gene expression programming wikipedia , lookup
Genome (book) wikipedia , lookup
Genomic imprinting wikipedia , lookup
Genetic drift wikipedia , lookup
Designer baby wikipedia , lookup
X-inactivation wikipedia , lookup
Microevolution wikipedia , lookup
Quantitative trait locus wikipedia , lookup
Chapter 10 Genetics: Mendel and Beyond Biology 101 Tri-County Technical College Pendleton, SC It’s a character trait  A character is a feature such as flower color  Best described as a gene  A trait is a particular form of a character, such as white flowers  Best described as an allele  A heritable character trait is one that is passed from parent to offspring  Before Mendel, blending was model of choice…and it was logical to a point Law of Segregation  Mendel and it’s all about flowers and sex  In sexually reproducing organisms, an individual possesses 2 “factors” for each trait  One came from mommy and one from daddy  When that individual makes gametes, those “factors” (alleles) will separate (segregate) from each other and wind up in different gametes  **Gamete receives only ONE member of the pair of alleles Defining Definitions  Genotype is genetic constitution of the organism  It’s what in the genes  Phenotype is the physical expression of the genotype  It’s what one sees—phenotype is the expression of genotype  Dominant means always expressed (in the phenotype)  Only one allele needed for its expression  DOES NOT MEAN “THE BEST TO HAVE” Definitions, cont.  Recessive means “covered”, “hidden”, or “masked” by presence of dominant allele  Recessive allele only expressed when present in pairs  Homozygous means “same” or two copies of same allele  Can be homozygous dominant or homozygous recessive  TT or tt, respectively Definitions, cont.  Heterozygous means “different” or “other”  Two different alleles of the “trait” (gene/allele) in question (Tt)  Monohybrid means differing in only ONE trait  tall or short; yellow or green, etc.  Dihybrid means differing in TWO traits  tall and yellow; short and green Monohybrid Cross  P = parental generation  F1 = first filial generation (first generation of hybrid)  F2 = second filial generation (second generation of a hybrid)  Punnett square is an application that allows prediction of probability of genotypes/ phenotypes from a genetic cross Test Cross  Test cross is dated concept that still serves useful purpose  Estes and the field of corn  Defined as mating an individual of unknown genotype with an individual homozygous recessive for the trait  Figure the Punnett square for this one…you will see it again!! Law of Independent Assortment  In dihybrid crosses, parental traits appear in new combinations of 2 of the phenotypic classes  such new combinations called recombinant phenotypes  Alleles of different genes assort independently of one another during gamete formation  In other words, T does not always stay with Y and vice versa  Law of Independent Assortment NOT as universal as law of segregation Independent Assortment, cont.  Applies to genes on separate chromosomes but not necessarily to those that lie on same chromosome  Simply states that chromosomes segregate independently during formation of gametes as do any two genes (alleles) on separate chromosome pairs Dihybrid Crosses  Review: dihybrid means two contrasting traits  TTYY crosses with ttyy  Do the Punnett square and look for 9 genotypes and 4 phenotypes  Be sure and remember the phenotypic ratio…you will see it again and again!!! Incomplete Dominance  When heterozygous phenotype is intermediate, gene is said to be governed by incomplete dominance/lack of dominance   Looks like blending to be sure Time for a Wally World story…Yeah!!!!  Red and white snapdragon cross produces all pink offspring    All F1 to self-fertilize and predict F2 Black rooster and white hen = all gray chicks Red bull and white cow = all roan calves To dominate…or Not  Complete dominance results when single allele produces enough protein to give maximum phenotypic response  Incomplete dominance results when heterozygotes show intermediate phenotype  Codominance results when two alleles at locus produce two different phenotypes that both appear in heterozygoes  Means both are fully expressed  Best example is ABO blood grouping ABO Blood Grouping  Blood type determined by proteins on surface of RBCs  Protein coded for by info in DNA  Alleles are IA and IB  There are six genotypes and four phenotypes  This is ABO only, we will discuss Rh factor  This one always gets me into trouble  Chalk talk time on ABO and Rh typing Linkage  Association between markers (genes/alleles) on same chromosome such that they do NOT show random assortment and seldom recombine  Closer the markers, lower frequency of recombination  Closer they are together, more likely they are to STAY together  MAP units Determining Sex  Sex (gender) determined by sex chromosomes (23rd pair)  Females are XX and males are Xy  AFAWK, only thing on y chromosome is SRY (male-determining) gene and gene for hairy ears  Nature was not overly kind to males  Implications of XX and Xy Sex-linked Disorders  Defined as being “tied” to X sex chromosome  Sex-linked disorders affect males more  One mutant recessive allele leads to redgreen colorblindness, muscular dystrophy, and hemophilia  Human mutations inherited as sex-linked dominant must LESS common than recessives Sex-linked, cont.  Dominants appear in every generation and individuals carrying harmful mutation (even as heterozygotes) often fail to survive and/or reproduce  Chalk talk time on hemophilia and/or color blindness