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124 Cards in this Set

  • Front
  • Back
The Austrian monk whose experiments with pea plants were the beginning of our understanding of genetics was _____________________.
Gregor Mendel
The different alternatives or choices for a gene (like blue, green, or brown eyes) are called _____________.
alleles
Crossing organisms from the F1 generation produces the _____ generation.
F2
Crossing organisms from the P1 generation produces the _____ generation.
F1
Mendel’s “factors” are now called ___________________.
genes
Self-pollination produces seeds with genetic information from _______ parent plant(s).
ONE
What pattern did Mendel see when crossing pure TALL with pure SHORT pea plants?
ALL the F1 offspring were tall, but 25% the F2 generation were short and 75% were tall.
If a dominant allele is present, the __________________ won’t be seen.
recessive allele
Pollen is produced by the _________________ part of the flower.
male
Dominant alleles are represented by a _______ case letter.
upper
Mendel’s Law of ____________ ____________ explains why alleles end up in different gametes following meiosis.
independent assortment
_______________________ A characteristic that can be observed such as hair color, seed shape, flower color, etc
Trait
_______________________ The joining of a sperm and egg to make a zygote
fertilization
_______________________ A gene choice that MASKS ANOTHER choice for a trait
dominant
_______________________ A gene choice that IS MASKED BY ANOTHER choice for a trait
recessive
_______________________ the branch of biology that studies how characteristics are transmitted from parent to offspring
genetics
_______________________ the passing of characteristics from parent to offspring
heredity
_______________________ An alternative choice for a gene (such as brown, green, or blue eyes)
allele
_______________________ An organism that always produces offspring identical to itself if self pollinated
pure breeding
What is the genotype of a HETEROZYGOUS YELLOW plant? ______________________
Yy
What is the genotype of A HOMOZYGOUS GREEN SEED plant? ______________________
yy
Make a cross between a PURE YELLOW SEED parent and a PURE GREEN SEED parent.

Genotypes of Parents: __________ X __________
YY x yy
POSSIBLE OFFSPRING OF CROSS BETWEEN TWO HOMOLOGOUS PAIRS (ONE DOMINANT, ONE RECESSIVE) GENOTYPES
HETEROZYGOUS (100%)
If you cross 2 parent plants that are BOTH HETEROZYGOUS for a trait the offspring will show a ____ : ____ phenotypic ratio.
________ % of the offspring will show the DOMINANT trait and
________ % of the offspring will show the RECESSIVE trait.
3:1
75
25
USE DOMINANT OR RECESSIVE TO FILL IN THE BLANKS BELOW:
¼ of the offspring will have two __________________ alleles, ½ will be hybrids with one _______________ and one _______________ allele, and
¼ will have two _________________ alleles.
recessive
dominant
recessive
dominant
MAKE A CROSS WITH 2 HETEROZYGOUS FOUR O’CLOCK PLANTS.
Genotypes___________________________ Genotypic Ratio ______________________
Phenotypes __________________________
Phenotypic Ratios _____________________
RR, rr, Rr
2:1:1
red,white,pink
2:1:1
You are exploring the jungle and find a new species of plant. Some of the plants have red flowers and some have yellow flowers. You cross a red flowering plant with a yellow flowering plant and all the offspring have orange flowers. You might assume that the alleles for flower color in this plant show ____________________.
incomplete dominance
If the red and yellow alleles in the mystery jungle plant above showed CODOMINANCE instead, what might you expect a plant with one red allele and one yellow allele to look like?
It would have red and yellow flowers together on one plant
SEE A PATTERN FOR HOMOZYGOUS DIHYBRID CROSSES:

If you cross plants that are PURE DOMINANT for TWO TRAITS with plants that are PURE RECESSIVE for TWO TRAITS, ________ % of the offspring will look DOMINANT for BOTH traits and the ________________ traits will not show at all.
100
recessive
genes: factors that __________________________ -- the part of the DNA molecule containing the genetic code
control organism traits
alleles:
different forms of a gene associated with a particular characteristic (ex. height : tallness/shortness)
chromosomes: ____________________________________________________________
hereditary units of an organism
locus:
particular point where a certain gene is found on a chromosome
homologous chromosomes:
pair of associated chromosomes -- each chromosome in the pair is called a homologue
** Mendel developed some basic principles of heredity ______________________________________. His principles of dominance, segregation, and independent assortment were established through the ________________________ of large numbers of offspring produced by crossing pea plants.
by breeding garden peas
mathematical analysis
** As a result of analyzing specific mathematical ratios associated with certain characteristics in the offspring, Mendel proposed that characteristics were ______________ as the result of the transmission of ____________________________________.
inherited
hereditary factors
•Every organism requires a set of coded instructions for specifying its traits. For offspring to resemble their parents, their must be a reliable way to ____________________________________________ from one generation to the next.
transfer hereditary information
•Each gene carries a separate piece of information. An inherited trait of an individual can be determined by one or by many genes, and a single gene can influence _______________________________________________.
more than one cell
** Alleles are located in _________________________________________________ on homologous chromosomes.
the same position as locus
B. In asexually reproducing organisms, all the genes come from a ______________________. These genes are normally _________________ to the parent. (clone)
single parent
identical
C. Sexually reproducing organisms normally receive half their genetic information from the Mother's egg and half their genetic information from their Father's sperm. Sexually reproduced offspring ____________________________ ___________________________________ to their parents.
resemble, but are not identical
Mendel's hereditary factors, now called _____, exist at definite loci in a linear fashion on chromosomes. Two genes associated with a specific characteristic are known as __________ and are located on homologous chromosomes. The gene-chromosome theory provides the mechanism to account for the hereditary patterns which Mendel observed.
genes
alleles
1. __________ breeding: When the plants self-pollinate, all their offspring are of the same variety.
True
2. Hybridization: Mating, or _____________, of two varieties.
crossing
3. Monohybrid cross: A cross that tracks the inheritance of a _______________ character.
single
. homozygous (pure) --
an individual with two of the same alleles on homologous chromosomes
heterozygous: (hybrid) --
an individual with contrasting alleles for the same trait on homologous chromosomes
__________________ generation (P) -- the two original organisms being crossed
Parental
first ______________ generation (F1) -- the first generation of offspring from the parents
filial
second filial generation (F2) --
generation of offspring arising from the first filial generation
The __________________________________________states that for contrasting traits only the dominant trait can be seen. Mendel saw this unfold for all of the seven traits that he studied.
law of dominance
Law of Dominance (Mendel)
a pattern of heredity in which only _______________________ of an allelic pair is expressed
one gene
Law of Dominance (Mendel)
In the heterozygous condition, one allele of a gene may express itself and mask the presence of the other allele: EX.
purple flowering X white flowering-->purple flowering peas
Law of Dominance (Mendel)
________________________ trait: the trait or allele that is expressed
dominant
Law of Dominance (Mendel)
recessive trait: the trait or allele that is present but that is _________________________________
masked by dominant trait
Law of Dominance (Mendel)
progeny --
offspring
Law of Dominance (Mendel)
siblings --
brothers or sisters
Law of Dominance (Mendel)
Punnett square:
used to represent genetic crosses
Law of Dominance (Mendel)
genotype: the _________________________________ of an organism
genetic makeup
Law of Dominance (Mendel)
phenotype: the __________________________ of an organism
physical characteristics
Mendel wanted to know why the recessive trait disappeared in one generation and reappeared in the next generation. He came up with the _________________________________________.
Principle of segregation and recombination
Principle of Segregation and Recombination (Mendel)
Principle of segregation and recombination states that
factors that occur in pairs are separated from each other during gamete formation and recombine at fertilization.
Principle of Segregation and Recombination (Mendel)
When gametes are formed during meiosis there is ______________________________________ of homologous chromosomes.
random segregation
Principle of Segregation and Recombination (Mendel)
As a result of fertilization, alleles recombine. As a consequence, new allelic gene ______________________ are likely to be produced.
combinations
** Segregation and recombination is illustrated by the cross between
two individuals heterozygous for a trait.
Law of Independent Assortment (Mendel)
If the genes for two different traits are located on different chromosomes (nonhomologous chromosomes), they segregate randomly during meiosis and, therefore, may be ____________________ ____________________________________________________________
inherited independently of each other
Law of Independent Assortment (Mendel)
The cross of two organisms heterozygous for a trait is known as a ________________ cross.
hybrid
** Assuming large numbers of two organisms heterozygous cross, the phenotypic ratio of dominant offspring to recessive offspring is ________ and the genotypic ratio of homozygous dominant offspring to heterozygous dominant offspring to homozygous recessive offspring is ___________
3:1
1:2:1
The laws of probability- In tossing a coin there is a ______ percent chance that a head will turn up. However, it is quite possible for you to toss a coin 10 times and obtain 8 heads and 2 tails. The law of probability is based on ____________________________.
50
sample size
number of trials
Test Cross-
To find out whether an individual showing a dominant trait is homozygous( TT ) or heterozygous ( Tt ) the individual can be crossed with another showing the recessive trait. ( tt ) If there are any recessive traits produced in the offspring the unknown parent must be ____________________.
heterozygous dominant
Monohybrid Cross-
A cross between individuals that involves one pair of contrasting traits

we use Punnett square diagrams to predict the results of various monohybrid crosses.
Dihybrid Cross-
a cross between individuals that involves two pairs of contrasting traits.
It is the simultaneous inheritance of two characteristics.
Predicting the results of a dihybrid cross is more complicated than predicting the results of a monohybrid cross.
All possible combinations of the four alleles from each parent must be considered.
Incomplete Dominance - A case of contrasting alleles in which one allele is only ______________ dominant over the other --the dominant allele is only partially expressed when the recessive
allele is present. Sometimes called ___________________ inheritance
partially
blending
Codominance: a case of contrasting alleles in which _________________________ is dominant over the other (alleles have equal power)
neither allele
Multiple Alleles
In some traits more than two alleles can exist in a population of a species, but a single individual can only possess _____ alleles.
two
Multiple Alleles
Ex: Human blood type has _________________ types.
four
Multiple Alleles
However there are ____________alleles that control blood types they are________________________.
three
A, B, AB, O
A and B are both ____________ over O.
dominant
Neither A nor B is _________ Over each other (codominant)
dominant
Which red blood cells surface proteins are found on: Type A,
A agglutinogens only
Which red blood cells surface proteins are found on: Type B,
B agglutinogens only
Which red blood cells surface proteins are found on: Type AB,
A and B agglutinogens only
Which red blood cells surface proteins are found on: Type O?
none
Which plasma antibodies are produced by: Type A,
B agglutinin
Which plasma antibodies are produced by: Type B,
A agglutinin
Which plasma antibodies are produced by: Type AB,
None
Which plasma antibodies are produced by: Type O?
A and B agglutinin
Which blood types can be given and donated for type A
Can give blood to A and AB
can receive blood from A and O
Which blood types can be given and donated for type B
Can give blood to B and AB
can receive blood from B and O
Which blood types can be given and donated for type O
Can give blood to AB, A, B, O (universal donor)
can receive blood from O
Which blood types can be given and donated for type AB
Can give blood to AB
can receive blood from AB, A, B, O (universal receiver)
gene linkage: when genes for two different traits (non-allelic genes) are located on the ________________________ pair (homologous chromosomes) - Linked genes are __________________ inherited together
same chromosome
usually
The exception to gene linkage can be found when ____________________________ occurs. For example not all persons with red hair have freckles. This variation from the expected normal may be due to crossing over.
crossing over
crossing over:
during synapsis in the first meiotic division, the chromatids in a homologous pair of chromosomes often twist around each other, break, exchange segments and rejoin
Crossing over results in the _____________________________ of linked genes and increases the variability of offspring.
rearrangement
• Sex linkage is the _______________ expression of an __________ that is dependent on the sex of the individual and is directly tied to the ______________________________.
phenotypic
allele
sex chromosome
In sex linkage there is a homogametic sex and a heterogametic sex. In mammals the homogametic sex is female (XX) and the heterogametic sex is male (XY), thus the sex linked genes are carried on the _____________________.
X Chromosome
• Sex-linked traits are inherited through chains of carrier ______________. That is, a girl, her mother, and her mother's mother all are carriers, while some of their sons have the trait.
mothers
• X-linked genes are ______________ passed from father to son. The Y chromosome is the only sex chromosome that passes from father to son.
never
• Males are never _______________ – if they have a mutated gene on the X chromosome, it will be expressed
carriers
To "read" a set of human chromosomes, scientists first use three key features to identify their similarities and differences:
________. This is the easiest way to tell two different chromosomes apart.
Size
To "read" a set of human chromosomes, scientists first use three key features to identify their similarities and differences:
________________. The size and location of Giemsa bands on chromosomes make each chromosome pair unique.
Banding pattern
To "read" a set of human chromosomes, scientists first use three key features to identify their similarities and differences:
_____________________ Centromeres are regions in chromosomes that appear as a constriction. They have a special role in the separation of chromosomes into daughter cells during mitosis cell division (mitosis and meiosis).
Centromere position.
Using these key features, scientists match up the ___ pairs -- one set from the mother and one set from the father.
23
____________________ chromosomes- the centromere lies near the center of the chromosome.
metacentric
____________________ chromosomes- chromosomes have a centromere that is off-center, so that one chromosome arm is longer than the other. When chromosomes are aligned, they are oriented so that the short arm, designated "p" (for petite), is at the top, and the long arm, designated "q" (simply for what follows the letter "p"), is at the bottom.
submetacentric
____________________ chromosomes- the centromere resides very near one end.
acrocentric
Down Syndrome
The effects of Down Syndrome vary greatly from person to person but can include mental retardation, eyes that slant upward, and heart defects.

People with Down Syndrome have 3 copies of chromosome 21. For this reason, Down Syndrome is also called "Trisomy 21".
Turner Syndrome
Symptoms include short stature and lack of ovarian development. Other features, such as webbed neck, arms that turn out slightly at the elbow, and a low hairline in the back of the head are sometimes seen.

Women and girls with Turner Syndrome have only one X chromosome. This is an example of monosomy.
Klinefelter’s Syndrome
People with this disorder develop as males with subtle characteristics that become apparent during puberty. They are often tall and usually do not develop secondary sex characteristics such as facial hair, or underarm and pubic hair.

Men and boys with Klinefelter Syndrome have a Y chromosome and 2 X chromosomes. This is an example of trisomy.
Reciprocal Translocation: Philadelphia chromosome
This translocation, which is found only in tumor cells, indicates that a patient has chronic myelogenous leukemia (CML). In CML, the cells that produce blood cells for the body (the hematopoietic cells) grow uncontrollably, leading to cancer.

This person has 46 chromosomes with a translocation of material between chromosome 9 and chromosome 22 (commonly known as the Philadelphia chromosome).
Cri du chat Syndrome
Cri du chat is a rare syndrome (1 in 50,000 live births) caused by a deletion on the short arm of chromosome 5. The name of this syndrome is French for "cry of the cat," referring to the distinctive cry of children with this disorder. The cry is caused by abnormal larynx development, which becomes normal within a few weeks of birth. Infants with cri du chat have low birth weight and may have respiratory problems. Some people with this disorder have a shortened lifespan, but most have a normal life expectancy.
Williams Syndrome
caused by a very small chromosomal deletion on the long arm of chromosome 7. The deleted region includes the elastin gene (see figures A and B below), which encodes a protein that gives blood vessels the stretchiness and strength required to withstand a lifetime of use. The elastin protein is made only during embryo development and childhood, when blood vessels are formed. Because they lack the elastin protein, people with Williams Syndrome have disorders of the circulatory system, also known as vascular disorders.
karyotype
a display of the chromosomes of a single cell. To obtain it, the cell is stained, then a picture is taken of it through a microscope just before cell division, when the chromosomes are easiest to see.
Nondisjunction– failure of chromosome ____________ during meiosis (during ________).
Causes gamete to have too _____ or too ____ chromosomes
to separate
anaphase
many or few
Deletion – due to breakage
A piece of chromosome is ______
lost
Insertions and Deletions: Extra base pairs may be added (_____________________) or removed (___________________) from the DNA of a gene. The number can range from one to thousands. Collectively, these mutations are called _________. _________ involving one or two base pairs (or multiples thereof) can have devastating consequences to the gene because translation of the gene is "_______________". The mRNA is translated in new groups of three nucleotides and the protein specified by these new codons will be worthless. A number of inherited human disorders are caused by the insertion of many copies of the same triplet of nucleotides. Huntington's disease and the fragile X syndrome are examples of such ___________ __________diseases. Huntington’s Disease- An incurable form of insanity that does not show up until the age of 35-40. This disease is rather unique because it is dominant!!
insertion

deletions

indels

indels

frameshifted

trinucleotide repeat
Nondisjunction– failure of chromosome ____________ during meiosis (during ________).
Causes gamete to have too _____ or too ____ chromosomes
to separate
anaphase
many or few
Translocation– Involves two chromosomes that aren't ____________.
Part of one chromosome is ___________ to another chromosome.
homologous

transferred
The _________ determines if the offspring will be male or female?
MALE
Which sex is homogametic?
female
Which sex is Heterogametic?
male
EPIGENETICS
changes in gene expression that are stable between cell divisions, and sometimes between generations, but do not involve changes in the underlying DNA sequence of the organism. Basically, it is a term used to describe the idea that environmental factors can cause an organism's genes to behave (or "express themselves") differently, even though the genes themselves don't change.
Pedigree
A Pedigree Chart is a chart which tells one all of the known phenotypes for an organism and its ancestors, most commonly humans, show dogs, and race horses.