chapter 20 and 21 Flashcards
certain segments of DNA
genes
different forms of a gene
alleles
one that has the ability to mask the expression of another
dominant allele
one whose expression is masked by the dominant allele for the same trait
recessive allele
an organism that has 2 identical alleles
homozygous
organism that has 2 different alleles
heterzygous
precise set of alleles a person possess for a given trait
genotype
observable physical trait or traits
phenotype
discovered laws of heredity
mendelian genetics
letters
genotype
individuals observable traits - height, eye color, blood type
phenotype
chart showing the genetic connections between individuals in a family
pedigrees
any chromosomes other than a sex chromosome
autosome
normal allele (a) is recessive and those with the alleles AA or Aa have the disorder
autosomal dominant
normal allele (A) is dominant and only those with the alleles aa have the disorder
autosomal recessive
Aa appear normal but can have a child with the disorder
carriers
marfan syndrome
autosomal dominant disorder
abnormal connective tissue
marfan syndrome
weakened brittle bones
osteogensis imperfecta
osteogensis imperfecta
autosomal dominant disorder
neurological disease
huntington disease
high cholesterol
familial cholesterolemia
huntington disease
autosomal dominant disorder
huntington disease
autosomal dominant
premature aging
progeria
progeria
autosomal dominant
very thick mucus in bronchial tubes and pancreatic ducts
cystic fibrosis
cystic fibrosis
autosomal recessive
albinism
autosomal recessive
sickle cell anemia
autosomal recessive
when there are more than 2 possible for a particular trait
multiple alleles
both expressed when both present
codominant
shown when heterozygote has intermediate phenotype between dominant and recessive homozygous
incomplete dominance
when a trait is controlled by 2 or more genes and each dominant allele has an additive effect to the phenotype
polygenic inheritance
XX
female
XY
male
determines sex of baby
male
has some genes on it that are unrelated to a gender
X chromosome
carries very few genes
Y chromosome
get 1 X chromosome and if they get recessive gene they show disorder
male
color blindness
X-linked disorder
muscular dystrophy
X-linked disorder
hemophilia
X-linked disorder
tests are available to detect or predict some genetic disorders
detecting genetic disorder
long needle inserted into abdomen to collect some amniotic fluid with living cells floating in it
amniocentesis
small amount of tissue containing part of the placenta is removed and analyzed for genetic abnormalities
chorionic villi sampling
blood test in newborns routinely to screen for
pku
may predictive genetic tests now available or being developed; blood tests
adult genetic testing
permanent change in the sequence of bases in DNA
gene mutation
what can gene mutations be from
change/swap in a single DNA nucleotide
inserted base
deleted base
example of gene mutation
sickle cell anemia- just one amino acid swapped in the hemoglobin protein
manipulation of genetic material for human purposes
genetic engineering
recombinant DNA contains DNA from 2 or more different sources
recombinant dna
e. coli is used to produce what
human insulin for diabetics
why is e. coli used in recombinant DNA
using an enzyme to cut an opening into bacterial DNA and inserting a human gene into it
used to create copies of segments of DNA quickly in a test tube
polymerase chain reaction
what are new copies of DNA fingerprinting used for
identifying and convicting criminals identifying bodies paternity suits detecting genetic disorders even recognizing illegally poached ivory and whale meat
genetic engineering
environmental- oil eating microbes for oil spills
livestock- vaccines for animals
pharmaceuticals- edible vaccines for hepatitis B- in bananas
agriculture- higher yields
used to cure genetic diseases
gene therapy
method of gene therapy
gene is inserted into cells that have been removed and then returned to the body
diseases of gene therapy
SCID, AIDS, muscular dystrophy, cystic fibrosis
study of our complete genetic makeup
genomics
how long did it take for genomics
13 yr effort completed in 2003
whats the purpose of genomics
discovered the order of the base pairs in human DNA
what did genomics determine
humans have 20,000-25,000 genes that code for proteins
base pairs of rna
adenine-uracil
cytosine-guanine