the human genome chapter 14-1 & 14-2. think about it what does a can of diet coke and this song...
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![Page 1: The Human Genome Chapter 14-1 & 14-2. THINK ABOUT IT What does a can of Diet Coke and this song have to do with human genetics? (Answers to come in this](https://reader038.vdocuments.mx/reader038/viewer/2022102818/56649d585503460f94a38277/html5/thumbnails/1.jpg)
The Human GenomeChapter 14-1 & 14-2
![Page 2: The Human Genome Chapter 14-1 & 14-2. THINK ABOUT IT What does a can of Diet Coke and this song have to do with human genetics? (Answers to come in this](https://reader038.vdocuments.mx/reader038/viewer/2022102818/56649d585503460f94a38277/html5/thumbnails/2.jpg)
THINK ABOUT IT
What does a can of Diet Coke and this songhave to do with human
genetics?(Answers to come in this slide show!)
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HUMAN GENETICSDominant and
Recessive
Homozygous/Heterozygous
work for human genes too!
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________ are made by joining___________ subunits togetheramino acid
Proteins
REMEMBER YOUR MOLECULES!
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REMEMBER YOUR MOLECULES
__________ is carried in the ________ of A, T, G, C’s on a_____ moleculeDNA
Genetic code
sequence
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The sequence of A’s, T’s, G’s & C’stells the _______ of ________ in the
________
ORDER amino acidsprotein
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Changes in the gene code _______________ that is made
A change in the genetic code =________________
MUTATION
change the protein
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KINDS OF MUTATIONS________ CELLS = ___________ CELLS
Somatic cell mutations can: ______________________
______________________
_____________
BODY
Cause cancer
Make cell not able to function
Kill cell
BUT _________ passed on to offspring
WON’T BE
SOMATIC
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Kinds of Mutations
___________ = _________cells(sperm & eggs)
GAMETES
Germ cell mutations ________ passed on to offspring
CAN BE
http://anthro.palomar.edu/biobasis/images/meiosis.gif
GERM
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____________- Most mutations have little or no effect on gene ____________.
_____________ in code can absorb many mutations without changing theamino acid sequence.
UUC and UUU bothcode for same amino acid
MUTATIONS can be:
NEUTRALfunction
REDUNDANCY
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____________ - Mutations that produce ______________ are usually harmful.
Harmful mutations are associated with many________________ and can cause____________
MUTATIONS can be:
HARMFULdefective proteins
genetic disorderscancer
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____________ - Some mutationschange proteins that are so vital to life that they cause death, usually before birth.
50% of pregnancies that abort spontaneously have genetic abnormalities
MUTATIONS can be:
LETHAL
http://www.global-warming-and-the-climate.com/images/tombstone-RIP.gif
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Mutations can help an organism _________________
Provide a way for species to changeover time
____________- Mutations are also a source of ______________ in thepopulation
MUTATIONS can be:
BENEFICIALgenetic variation
survive and reproduce
MORE ON THIS2nd SEMESTER!
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Mutations can happen:• when cells make_________ in copying DNA• when cells are exposed to environmental ___________ like __________- X-rays, tanning booths
__________ - cigarette smoke, pollutants__________ - HPV
_______________ are changes in the genetic material.MUTATIONS
mistakes
REMEMBER!
carcinogensradiationchemicalsviruses
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Mutations that produce changes in a single gene = _________________
Mutations that produce changes in whole chromosomes = _____________________
KINDS OF MUTATIONS
GENE MUTATIONS
CHROMOSOMAL MUTATIONS
Images from: http://www.bbc.co.uk/scotland/education/bitesize/higher/img/biology/genetics_adaptation/mutations/02gene_mutation.gif
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MANY HUMAN GENES HAVE BECOME
KNOWN THROUGH THE STUDY OF GENETIC DISORDERS
Many genetic ___________ result fromchanges in the DNA code so
_________________ proteins are produced.
DISORDERS
NON-FUNCTIONING
http://patentdocs.typepad.com/photos/uncategorized/2007/05/28/dna1.gif
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A mutation that causes a protein to beNON-FUNCTIONAL would appear_______________ to the normal working allele.
Examples of __________________________ GENETIC DISORDERS: (autosomes-22 non-sex chromosomes)____________________
____________________
____________________
RECESSIVE
PHENYLKETONURIA (PKU)
TAY-SACHS DISEASE
CYSTIC FIBROSIS
AUTOSOMAL RECESSIVE
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Phenylketonuria (PKU)
CAUSE: Mutation in gene for an ___________ that __________ an ___________ called phenylalanine
Build up causes ________________________MENTAL RETARDATION
ENZYME
http://biology.clc.uc.edu/courses/bio104/protein.htm
breaks down amino acid
X
X
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Phenylketonuria (PKU)
____ babies are ________for PKU before they leave the hospital.
Treatment: Need a diet _____________________ to extend life and ______________ mental retardation
If phenylalanine is an _____________, what type of foods should PKU patients avoid? __________________
amino acid
PROTEINS !
LOW in phenylalaninePREVENT
ALL tested
http://labspace.open.ac.uk/file.php/2588/SK195_6_002i.jpg
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THINK ABOUT IT
What does a can of Diet Coke have to dowith human genetics?
LOOK AT THE WARNING LABEL !
______________ is made with phenylalanineNUTRASWEET
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TAY-SACHS DISEASE___________________
CAUSE: Mutation in gene for an ___________ that breaks down a kind of _________in the developing _________
Build up of lipids in brain cells leads to:mental retardation, blindness, and DEATH in early childhood
Found more frequently in people with _______ _____________ ______________, ancestry
BRAIN
ENZYME
Jewish
Image from: http://www.djsfoundation.org/images/Steeler%20pics%20Dylan.jpg
AUTOSOMAL RECESSIVE
Mediterranean Middle Eastern
LIPID
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http://www.biochem.arizona.edu/classes/bioc460/spring/rlm/RLM36.1.html
A __________ person who carries a _________ allele for a genetic disorder, but ______________ the disorder themselves is called a_____________CARRIER
heterozygous
doesn’t show
recessive
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CYSTIC FIBROSIS CAUSE:
Loss of 3 DNA bases in a gene for the _____________ that transports _________ so salt balance is upset
Causes a build up of _________________ in lungs and digestive organs
.
thick mucous
protein
Image from: BIOLOGY by Miller and Levine; Prentice Hall Publishing ©2006
Cl- ions
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REMEMBER TRANSPORT
_____________ are membrane proteins that make _________ through the bilayer for ____ to pass through (Na+, K+, Ca++, Cl-)
ION CHANNELS
tunnelsions
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CYSTIC FIBROSIS
http://learn.genetics.utah.edu/content/disorders/whataregd/cf/index.html
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CYSTIC FIBROSISLeads to: _________ and _________ complications, increased susceptibility to infections;
“__________” is a symptom
More common in ____________ but can affect all races.
30,000 people in U.S. have cystic fibrosis
1 in 31 people are carriers
Caucasians
respiratory digestive
Salty skin
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A mutation that codes for a new proteinwhose action masks the normal alleleappears as a ______________ mutation.
Examples of _________________________ GENETIC DISORDERS:
____________________
____________________
DOMINANT
Huntington’s disease
Achondroplasia
AUTOSOMAL DOMINANT
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HUNTINGTON’S DISEASE______________________
CAUSE: Extra 40-100 ______________ at end of gene on chromosome 4
The _____________ . . . the more __________ the symptoms.
severe
CAG repeats
http://www.healthsystem.virginia.edu/internet/huntdisease/images/cag.gif
more repeats
AUTOSOMAL DOMINANT
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HUNTINGTON’S DISEASE
Causes progressive _____ of ________________ and ___________function
loss
muscle control
mental
1 in 10,000 people in U.S. have Huntington’s disease
http://www.scielo.br/img/revistas/bjmbr/v39n8/html/6233i01.htm
Huntington’s brain
Normal brain
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A person with Huntington’s disease has a _____ chance of passing the disorder on totheir offspring.
Problem:Symptoms of disorder usually don’t show until ____________ . . .
so you don’t know you have it until ________ you have had children.
50%
MIDDLE AGE
AFTER
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THINK ABOUT IT
What does the songhave to do with human genetics?
“This Land is My Land” was written by a musician named Woody Guthrie before he began to show the symptoms of Huntington’s disease.
Click to hearWoody’s song
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Woody Guthrie had a son named Arlo that was a popular musician during the 70’s
Before 1993 there was no test for Huntington’s.
If one of your parents showed symptoms, you had to wait to see if it had been passed on to you.
Click to hear one of Arlo’s songs
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Arlo Guthrie is still performing today.
He never developed symptoms for Huntington’s disease.
http://www.jimdirden.com/woodyfest2004/artists/index_3.htm
If there is no cure, would YOU want to be tested and find out if you have the gene?
http://webs.wichita.edu/depttools/depttoolsmemberfiles/accomp/question_mark%20(WinCE).jpg
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ACHONDROPLASIA(One kind of Dwarfism)
CAUSE: ___________________________ gene
200,000 “little people” worldwide
One of oldest known disorders – seen in Egyptian art
AUTOSOMAL DOMINANT
1 in 20,000 births
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ACHONDROPLASIA(One kind of Dwarfism)
Normal size head and torso; short arms and legs
Problem with way cartilage changes to bone as bones grow
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DISORDERS CAUSED BY ____________________
____________________SICKLE CELL DISEASE
CAUSE: T changed to A in gene for
__________________ (protein in red blood cells that carries oxygen in blood)
HEMOGLOBIN
AUTOSOMAL CODOMINANT ALLELES
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SICKLE CELL DISEASE
SYMPTOMS:_____________ become sickle shaped in persons with ______ sickle cell ________
RED BLOOD CELLS
TWOALLELES
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SICKLE CELL DISEASE
Circulatory problemsCells stick in capillariesLoss of blood cells (anemia)Organ damage (brain, heart, spleen)Can lead to DEATH
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SICKLE CELL DISEASEMore common in _________________ 1 in 500 = have sickle cell disease 1 in 10 = carriers for allele
Also affects persons of _______________ and _________________ descent
Why do so many African Americans carry the sickle cell allele?
AFRICAN AMERICANS
MEDITERRANEANMIDDLE EASTERN
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SICKLE CELL DISEASEMany can trace their ancestry to
westcentral Africa where ___________,a serious parasitic disease thatinfects red blood cells is common.
Images from: http://en.wikipedia.org/wiki/Malaria
MALARIA
Watch a video about sickle cell and malaria
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A person who is __________________ for the ____________allele (ss) will have _______________
A person who is _________________ for normal hemoglobin alleles will have normal blood cells, but can become infected with __________ (SS)
A _________________ person (Ss)(with one normal/one sickle cell allele) isgenerally healthy and has the benefit ofbeing _________ to malaria
HOMOZYGOUSsickle cell
sickle disease
HOMOZYGOUS
malaria
HETEROZYGOUS
resistant
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A __________ is a picture of an organism’s chromosomes
KARYOTYPE
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Chromosomes that determine the sex of an organism = _________________
All other chromosomes = _________________
Sex chromosomes
autosomes
Humans have two sex chromosomes
and _____ autosomes
X y44
http://www.angelbabygifts.com/
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SEX DETERMINATIONXX =
Xy =
female
male
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Who decides?
Mom can give X
Dad can give X or y
SO ____ determines sex of the baby.
If dad gives X with mom’s X = girlIf dad give y with mom’s X = boy
X X
X
y
X X X X
X y X y
Dad
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_______________are diagrams that show how are ____________ on __________ over several generations
PEDIGREESgenes are passed
in families
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Drawing a pedigree chart
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http://www.beavton.k12.or.us/sunset/academics/genetics.htm
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http://www.ikm.jmu.edu/Buttsjl/ISAT493/Hemophilia/hemophiliaeurope.html
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SEX CHROMOSOMES CAN CARRY OTHER GENES TOO= ___________________SEX LINKED TRAITS
These traits show up in different _______________ in males and females because they move with the sex chromosomes
percentages
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Y-LINKED GENES: Genes ______________ chromosome
EXAMPLE:Hairy pinna
_________genes _____ show up _______Y linked in males
carried on Y
ONLY
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____________ GENES: are carried on the X chromosome
X-linked recessive disorders show up _____________in ______ than femalesbecause males only have______ X chromosome.
MALES
X-LINKED
ONE
MORE frequently
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Males ONLY HAVE ONE X
They eitherhave the disorder
DEFECTIVE NORMAL
They are normal
Or
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FEMALES HAVE TWO X CHROMOSOMES
Females have one normalgene that works.
NORMAL DEFECTIVEDEFECTIVE
Females __________defective recessivealleles to show the disorder
need 2
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The X chromosome in males . . . flies WITHOUT a copilot!
. . . there’s NO BACK UP X to help them!
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Examples of ________________________ DISORDERS:
____________________
____________________
____________________
HEMOPHILIA
COLORBLINDNESS
DUCHENNE MUSCULAR DYSTROPHY
X-LINKED RECESSIVE
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HEMOPHILIA CAUSE:
Mutation in genes for __________________ carried ______ chromosome
Blood clotting proteins are missing so person with this disorder can’t stop bleeding when injured; can ________________ from minor cuts or suffer internal bleedingfrom bruises or bumps.
bleed to death
Blood clotting proteinson X
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HEMOPHILIA Treatment:
Need ____________ of normal clotting proteins to stop bleeding
_____________ in ______ because it is X-linked, but females with ______ recessive hemophilia alleles will also show the trait.
1 in 10,000 males has hemophilia
injections
malesTWO
More common
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COLORBLINDNESS CAUSE:
Mutation in one of three genes for _______________ carried on X chromosome
Persons with this disorder have trouble distinguishing colors.
_________________ colorblindness is most common
Seen in 1 in 10 males 1 in 100 females
Red-green
Color vision
http://gizmodo.com/gadgets/peripherals/samsung-develops-lcd-for-colorblind-036306.php
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Duchenne Muscular DystrophyCAUSE: deletion in genethat codes for a_______________
Results in ____________________and loss of
___________________
http://www.cadenhead.org/workbench/gems/jerry-lewis-telethon.jpghttp://www.tokyo-med.ac.jp/genet/chm/dei.gif
muscle protein
progressive weakeningskeletal muscle
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Duchenne Muscular Dystrophy (DMD)
SYMPTOMS: 1 in 3000 male births Appears before age 5 Progressive muscle weakening Most in wheelchair by age 13 Eventually lethal
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What’s the pattern: ________ traits show up _______ in _______
__________________ traits: ______________________ than females. ________________ can be ________.
_______________________ traits:BOTH ______ & _________ can be ________
Y-linked ONLY males
X-linked recessivemore common in males
AUTOSOMAL RECESSIVE
ONLY FEMALES carriers
MALES FEMALES carriers
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________________ Abnormalities
• 1 infant in 200 newborns has a chromosomal abnormality • 28% of first trimester miscarriages have a chromosomal abnormality
• Abnormalities in larger chromosomes don’t usually survive
CHROMOSOMAL
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____________________________:Change in the ______________ or ____________ of chromosomes
CHROMOSOMAL MUTATIONS
structurenumber
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Homologous chromosomes ________________ during MEIOSIS
= _________________________
One cell gets 2 copies of the chromosome the other cell gets none.
NONDISJUNCTION
fail to separate
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Normal Meiosis Nondisjunction
http://www.tokyo-med.ac.jp/genet/anm/domov.gif
http://web.udl.es/usuaris/e4650869/docencia/gen_etica/meioferti2.html
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Nondisjunction
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NondisjunctionSince it happens to a
sperm or egg, the new
baby can end up
with _____________ of a
chromosome
= __________________
OR
only ___________ of a
chromosome
= ___________________
TRISOMY
MONOSOMY
3 copies
one copy
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Human Abnormalities caused by Non-Disjunction______________________________________________________
Down syndrome
Klinefelter syndrome
Turner syndrome
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Down syndrome (= ____________)TRISOMY 21
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Down syndrome (Trisomy 21)
• 1 in 800 births
• Similar facial features
• Slanted eyes
• Protruding tongue• Simian Line on Palm
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Down syndrome (Trisomy 21)
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Down syndrome (Trisomy 21)• Most common chromosomal
abnormality
• 50% have heart defects that need surgery to repair
• Mild to severe mental retardation
• Increases susceptibility to many diseases
• Risk of having a child with Down syndrome increases with age of mom
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Down syndrome (Trisomy 21)• Risk of having a child
with Down syndrome related to age of mom
• More common in women UNDER 16 or OVER 35
Cells that make eggs start meiosis in embryoStop in PROPHASE I (synapsis)One egg restarts & finishs division each monthSo an egg released at age 40 has been in synapsis for 40 years . . . chromosomes more likely to “stick”
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Turner syndrome
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Turner syndrome ____
• 1 in 5000 births• Females have only one X chromosome• Small size• Slightly decreased intelligence• 35% have heart abnormalities• Hearing loss common• Broad chest• Reproductive organs don’t develop at puberty• Can’t have children
http://medgen.genetics.utah.edu/photographs/diseases/high/611.gif
XO
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Klinefelter syndrome XXy
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Klinefelter syndrome
• 1 in 1000 births
• Males have extra X chromosomes
(Can be XXy, XXXy, or XXXXy)
• Average to slight decrease in intelligence
• Small testes/can’t have children
• Usually not discovered until puberty when don’t mature like peers
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Karyotype(need cells from baby)
Can tell __________________ chromosomes__________Some _____________________Can’t see _______________ mutations
Image from: http://members.tripod.com/~yenial/chromosome.html
MISSING/EXTRAGENDER
DELETIONS/INSERTIONSsingle gene
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If having extra chromosomes causes genetic problems, how
come having two X chromosomes in females and
one X in males is not a problem?
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X-chromosome Inactivation
In female cells ______ chromosome is randomly ________________
It condenses and forms a dense region in the nucleus called a
_____________BARR BODY
http://fig.cox.miami.edu/~cmallery/150/gene/barr.htm
ONE XSWITCHED OFF
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In some female cells the X with the allele for orange spots is switched off and in some cells the X with the allele for black spots is switched off, so cat has different colored spots.
CAT COLORIn cats, a gene that
controls the _____________
is carried on the
____________________X chromosome
http://www.islandstrolling.com/mainland/peloponnes/photo/mystra_cat_white_orange_black.jpg
SPOT COLOR
See a video
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_________ cats have only one X chromosome, so they can only have ____________ of spots!
CAT COLOR
Male
one color
http://ascensionparish.net/forum/messages/14/2493.jpg
THINK ABOUT IT?How many colors of spots could a male cat withKlinefelter syndrome have?
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MAKING TWINS
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___________ + ____________
_____________________________ _________________________________________ DNA ________________ DNA
Mom’s egg Dad’s sperm
___________ZYGOTE
MONOZYGOTIC =IDENTICAL
DIZYGOTIC = fraternalDIFFERENT
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_______________TWINSBabies are born __________ to each other
CONJOINED
attached