genetics exam 3

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196 Terms

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chromatin

DNA that’s packaged by proteins called histones; can exist in varying degrees of folding/compaction

eukaryotic cells only

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condensation

the process of compacting and organizing chromatin during cell division

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histones

basic proteins that package and compact DNA into structural units

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nucelosomes

a complex of eight histone proteins

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euchromatin

looser and more open; higher levels of transcription

<p>looser and more open; higher levels of transcription</p>
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heterochromatin

more compacted, much less transcription (genes are silenced)

<p>more compacted, much less transcription (genes are silenced)</p>
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histone acetylation

a reversible process where acetyl groups are added to lysine residues on histone tails; regulates gene expression and chromatin structure, causing the chromatin to become more open

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RNA interference(RNAi)

a biological process in which small pieces of RNA can shut down protein translation by binding the mRNAs that code for those proteins

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double-stranded RNA (dsRNA)

required for silencing

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short interfering RNA (siRNA)

20-22 nucleotides with a 3’ overhang; enters the RNA induced silencing complex and unzips the dsRNA

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mRNA degredation

after the single-stranded mRNA finds a complementary strand, it gets cut up by siRNA, causing its degredation

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Is transcription active or inactive in euchromatin?

euchromatin is transcriptionally active

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In what way does acetylation alter transcription activity?

Acetylation promotes transcription by neutralizing the positive charge of histone tails, weakening their interaction with DNA and making chromatin more accessible to transcription machinery.

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true-breeding

pollination results in 100% of the parent phenotype for all filial levels

<p>pollination results in 100% of the parent phenotype for all filial levels</p>
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alleles

alternative forms (variants) of a gene

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trait

a specific characteristic or feature of an organism that’s genetically determined

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homozygous

genotype with two alleles that are the same (SS, ss)

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heterozygous

genotype with two alleles that are different (Ss)

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dominant trait

a trait that is displayed by an individual that is heterozygous

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recessive trait

a trait that is not displayed by an individual that is heterozygous

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monohybrid cross

a genetic cross between two true breeding individuals that differ in only one trait; allows for the study of the inheritance patterns of a single gene

<p>a genetic cross between two true breeding individuals that differ in only one trait; allows for the study of the inheritance patterns of a single gene</p>
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dihybrid cross

a genetic cross between two individuals with two observed traits that are controlled by two distinct genes

<p>a genetic cross between two individuals with two observed traits that are controlled by two distinct genes</p>
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test cross

a genetic cross of an individual organism of dominant phenotype but unknown genotype and an organism with a homozygous recessive genotype/phenotype

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law of segregation (Mendel’s 1st law)

  • during gamete formation, the two alleles for one trait seperate from one another

  • at fertilization, only one allele is inherited from each parent, and allele choice is random

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law of independent assortment (Mendel’s 2nd law)

during gamete formation, alleles for different traits assort independently

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product rule

for independent events A and B, the probability of both A and B occuring is the product of their individual probabilities [p(A and B) = p(A) x p(B)]

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sum rule

the probabi;ity of either event A or event B occurring is the sum of their individual probabilities [p(A or B) = p(A) + p(B)]

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family pedigrees

a visual representation of a family’s genetic history highlighting relationships and patterns of inheritance for specific traits and conditions

<p>a visual representation of a family’s genetic history highlighting relationships and patterns of inheritance for specific traits and conditions</p>
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hallmarks of pedigrees for dominant traits

  • dominant traits can be displayed by an individual who is heterozygous or homozygous

  • affected individuals always have an affected parent

  • trait shows up at every generation - vertical pattern

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hallmarks of pedigrees for recessive traits

  • affected individuals are always homozygous

  • affected individuals can have two unaffected parents

  • when rare, recessive traits can appear without family history - horizontal pattern

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“carrier” for an allele

an individual who has a particular allele; term most often used for individual who has the allele but does not show the trait

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At a biochemical level, how can we explain the smooth or wrinkled pea phenotypes? Why is the smooth trait dominant and the wrinkled trait recessive?

The S (smooth) allele allows for translation of SBE1 which builds up branched starch in the organism, allowing it to retain water better. The s (wrinkled) allele does not allow for formation of branched starch and is therefore unable to retain water as well.

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Heterochromatin is…

a. more condensed

b. less condensed

a. more condensed

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A short interfering RNA (siRNA) triggers RNAi. This molecule is…

a. single-stranded, antisense

b. single-stranded, sense

c. double-stranded

c. double-stranded

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According to Mendel, a parent possess how many “particles” (alleles) of information for a trait?

a. 1

b. 2

c. 3

b. 2

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According to Mendel, how many alleles for a trait does a parent pass along to their child?

a. 1

b. 2

c. 3

a. 1

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True or False

Heterochromatin is an open structure that leads to transcription activation.

False

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True or False

Euchromatin does allow for gene transcription.

True

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True or False

DNA is wrapped around proteins called nucleosomes.

True

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How many histone proteins compose a nucleosome?

a. 2

b. 6

c. 8

d. 10

c. 8

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True or False

Histone tails are acetylated to convert heterochromatin into euchromatin.

True

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True or False

Fire and Mello’s experiment concluded that double-stranded RNA stimulates gene silencing.

True

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What is a structural characteristic of siRNA?

a. 20-22 nucleotides long

b. double-stranded RNA

c. 3’ overhang

d. all of the above

d. all of the above

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True or False

In RNAi, short interfering RNAs are designed to complement the target sequence/gene they must silence.

True

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In eukaryotic genomes, regions of _____ are transcriptionally active while regions of _____ are transcriptionally silent.

a. heterochromatin, euchromatin

b. euchromatin, heterochromatin

c. none of the above

b. euchromatin, heterochromatin

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True or False

We would expect histones with euchromatin to be acetylated.

True

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Which of the following is NOT a method of eukaryotic gene regulation?

a. histone acetylation

b. chromatin compaction

c. RNA interference

d. all of the above are methods of eukaryotic gene regulation

d. all of the above are methods of eukaryotic gene regulation

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In eukaryotes, histone acetylation leads to:

a. no change in chromatin organization

b. chromatin condensation

c. chromatin decondensation

c. chromatin decondensation

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Which of the following is true of a short interfering RNA (siRNA)?

a. short length (19-22 nt)

b. 3’ overhangs on each end

c. RNA-RNA base-pairing

d. all of the above

d. all of the above

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The molecule that triggers RNA interference is:

a. single-stranded sense RNA

b. single-stranded antisense RNA

c. double-stranded RNA

d. none of the above

c. double-stranded RNA

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True or False

In eukaryotes, some mRNAs are not translated because they are silenced by RNA interference.

true

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chromosome

a thread-like structure made of DNA and protein

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haploid

a cell containing one of each chromosome (1n)

<p>a cell containing one of each chromosome (1n)</p>
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diploid

a cell containing two of each chromosome (2n)

<p>a cell containing two of each chromosome (2n)</p>
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homolog (or pair of homologs)

pairs of chromosomes that have the same genes in the same order, but may have different alleles of those genes

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chromatid

one of the two identical halves of a homologous pair that has been replicated in preparation for cell division

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sister chromatids

the two identical copies of a single replicated chromosome that are formed during DNA replication; separated during cell division

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centromere

constricted regions on chromosomes that serve as the attachment point for spindle fibers and linking sister chromatids

<p>constricted regions on chromosomes that serve as the attachment point for spindle fibers and linking sister chromatids</p>
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chromosome arm

two arms on a chromosome that are separated by the centromere

<p>two arms on a chromosome that are separated by the centromere</p>
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crossover

exchange of the arms of the chromosomes between two homologous chromosomes’ non-sister chromatids; meiosis only

<p>exchange of the arms of the chromosomes between two homologous chromosomes’ non-sister chromatids; meiosis only</p>
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Cohesin protein

a protein that holds together the two chromosomes of a sister chromatid (shown in yellow on slides)

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Separase enzyme

“pac-man” enzyme that cuts cohesin once spindle tension is present

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segregation

meiosis reduces the chromosome number by half, allowing for only one homolog per gamete

<p>meiosis reduces the chromosome number by half, allowing for only one homolog per gamete</p>
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spindles

attach to the centromere and pull sister chromatids and individual chromosomes apart during mitosis and meiosis

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microtubule organizing centers

a cellular structure that nucleates and organizes microtubules

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S phase

part of the cell cycle where DNA replication occurs, ensuring each daughter cell receives a complete set of chromosomes

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mitosis

a type of cell division that produces two identical daughter cells from one parent cell; maintains chromosome number; haploid and diploid cells can unde

<p>a type of cell division that produces two identical daughter cells from one parent cell; maintains chromosome number; haploid and diploid cells can unde</p>
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meiosis I

sister chromatids exchange arms (crossovers) between homologs; each pair of homologs attached to both poles and aligned at cell equators; regulated cutting of cohesin at arms via separase enzyme

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meiosis II

sister chromatids align at equator and separate

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daughter cell

either of the two cells formed when a cell undergoes mitosis

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gamete

eggs and sperm; a haploid cell

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What is segregated at mitosis?

sister chromatids

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Describe the products of mitosis (include picture)

two genetically identical daughter cells

<p>two genetically identical daughter cells</p>
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What is segregated at each phase of meiosis? What are the products of meiosis?

1) homologous pairs separate producing two haploid cells

2) sister chromatids separate to produce four haploid daugter cells

<p>1) homologous pairs separate producing two haploid cells</p><p>2) sister chromatids separate to produce four haploid daugter cells</p>
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What happens in meiosis that allows a doubly heterozygous parent to produce gametes with all possible combinations?

Crossovers and alternative alignments

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<p>This trait must be…</p><p>a. dominant</p><p>b. recessive</p><p>c. could be either</p>

This trait must be…

a. dominant

b. recessive

c. could be either

b. recessive

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<p>Both parents must be…</p><p>a. homozygous</p><p>b. heterozygous</p><p>c. could be either</p>

Both parents must be…

a. homozygous

b. heterozygous

c. could be either

b. heterozygous

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The probability of producing a Smooth pea from a cross between heterozygous parents is…

a. 0.25

b. 0.50

c. 0.75

d. 1.00

c. 0.75

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True or False

Alleles are alternative forms of genes.

true

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In eukaryotes, how many total alleles does an individual possess per trait?

a. one

b. two

c. three

d. four

b. two

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In eukaryotes, how many total alleles does an individual receive from a parent?

a. one

b. two

c. three

d. four

a. one

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What term refers to the combination of alleles that an individual possesses?

a. phenotype

b. genotype

b. genotype

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True or False

A phenotype corresponds to an observable trait or characteristic.

true

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True of False

If an individual has a homozygous genotype, that means both alleles are different.

false

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Which law explains how members of different gene pairs are independently assorted into each gamete?

a. Mendel’s first law

b. Mendel’s second law

b. Mendel’s second law

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Which of the following statements explains Mendel’s first law?

a. two alleles for one trait will separate from each other

b. only one allele is randomly inherited from each parent

c. both statements are correct

d. neither statement is correct

c. both statements are correct

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True or False

In dominant traits, a heterozygous individual WILL display the trait.

true

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True or False

Wild-type traits will always be dominant.

false

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True or False

An autosomal trait is a trait located on a sex chromosome.

false

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Which of the following is a hallmark of recessive traits in pedigrees?

a. affected individuals are always homozygous

b. affected individuals may be heterozygous or homozygous

a. affected individuals are always homozygous

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Which of the following is another hallmark of a recessive trait in pedigrees?

a. affected individuals always have an affected parent

b. affected individuals can have two unaffected parents

b. affected individuals can have two unaffected parents

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Pedigrees that express a dominant trait display

a. vertical pattern

b. horizontal pattern

c. no pattern

a. vertical pattern

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hallmarks of X chromosome-linked traits

an allele located on the X chromosome

  • affected father will never pass to sons

  • affected father will pass allele to all daughters

  • males only have 1 x-linked allele so they will display the recessive trait

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parental type

progeny with the same allele combination as either parent

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recombinant type

progeny with a different allele combination than both parents

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recombination frequency (RF)

measures the likelihood of two genes being separated during meiosis

RF = (# recombinant progeny / # total progeny) x 100

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unlinked and linked genes

when two alleles are linked, they tend to be inherited together

rule for linked genes: # parental > > > # recombinant

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map unit

measure of distance between two genes on the chromosome

1% RF = 1 map unit

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single crossover

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double crossovers