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WorksheetsLecture Exam 3 Review
Total questions: 214
Worksheet time: 2hrs 47mins
The ability to reproduce in kind is a property of all living things.
True
False
Which type of reproduction requires fertilization (sperm and egg to fuse)?
Binary Fission
Sexual
Asexual
Budding
If a cell is described as 2N it is a _________ cell.
polyploidy
haploid
aneuploidy
diploid
If a cell is described as n it is a _______ cell.
haploid
diploid
polyploidy
aneuploidy
Sex cells are known as (sperm and eggs)
somatic
gametes
Skin, stomach, and nerve cells are known as
somatic
gametes
Which of the following is NOT an advantage of asexual reproduction?
no mate needed
offspring are identical to parents
genetic variation
reproduces quickly
The Red Queen hypothesis describes all the following except...
with no variations in the gene pool adaption will take place
no species can get too far ahead of other species
every small advantage gives a species an "edge"
all species coevolve
species that can't keep up go extinct
Before replication, germ cells have how many chromosomes?
23
46
92
After replication, germ cells have how many chromatids?
23
46
92
After meiosis, gamete cells have how many chromatids?
23
46
92
In sexual reproduction where do the chromosomes come from
all chromosomes come from one parent
chromosomes are randomly dispersed until the correct number is achieved
one chromosome comes from each parent
chromosomes come from sisters
Mitosis produces ______ daughter cells that are identical to the parent cell.
one
two
three
four
Meiosis produces ______ daughter cells that are unique from each other and the parent cell.
one
two
three
four
What cell is used to produce gametes?
skin
brain
germ
gametic
Mitosis has how many rounds of division (enter number)?
(a)
Meiosis has how many rounds of division (enter number)?
(a)
Mitosis produces cells that are
haploid
diploid
Meiosis produces cells that are
haploid
diploid
Before mitosis or meiosis, what stage must take place?
Cytokinesis
Interphase
Meiosis I
Meiosis II
DNA Replication takes place before both meiosis I and meiosis II.
True
False
Select the processes that take place during meiosis that contribute to genetic variation
independent assortment
homologous chromosomes separating
sister chromatids separating
crossing over
Crossing over takes place during
Prophase I
Metaphase I
Prophase II
Metaphase II
Independent assortment takes place in
Metaphase I
Anaphase I
Metaphase II
Anaphase II
Meiosis I is all about separating
sister chromatids
chromosomes
homologous chromosomes
centrioles
Meiosis II is all about separating
sister chromatids
chromosomes
homologous chromosomes
centrioles
Which round of meiosis is similar to mitosis?
Meiosis I
Meiosis II
Meiosis reduces chromosome number by half. This is why it is referred to as a _________________ process.
reduction
difficult
reductional division
dividing
Identify the phase where chromosomes condense, nuclear envelope disappears, spindles form, and crossing over takes place.
Prophase I
Metaphase I
Anaphase I
Telophase I and Cytokinesis
Identify the phase where pairs of homologous chromosomes move to the equator.
Prophase I
Metaphase I
Anaphase I
Telophase I and Cytokinesis
Identify the phase where pairs of homologous chromosomes move away to the opposite parts of the cell.
Prophase I
Metaphase I
Anaphase I
Telophase I and Cytokinesis
Identify the phase where pairs of homologous chromosomes gather at the poles and cytoplasm splits into two cells.
Prophase I
Metaphase I
Anaphase I
Telophase I and Cytokinesis
Identify the phase where spindles form, nucleus disappears, and centrioles move to the poles.
Prophase II
Metaphase II
Anaphase II
Telophase II and Cytokinesis
Identify the phase where sister chromatids line up at the equator.
Prophase II
Metaphase II
Anaphase II
Telophase II and Cytokinesis
Identify the phase where sister chromatids move away to the opposite ends of the cell.
Prophase II
Metaphase II
Anaphase II
Telophase II and Cytokinesis
Identify the phase where nucleus reforms, spindle breaks down, and cytoplasm splits to produce a total of 4 cells.
Prophase II
Metaphase II
Anaphase II
Telophase II and Cytokinesis
When homologous pairs line up in close interaction it is called
chiasma
synapsis
centromere
kinetochore
When homologous chromosomes exchange genetic material they are referred to as ______________ chromosomes.
changed
sister chromatids
non-recombinant
recombinant
Some homologous chromosomes exchange genetic material and some do not. When they don't exchange genetic material they are referred to as ______________ chromosomes.
changed
sister chromatids
non-recombinant
recombinant
The point of contact where non-sister chromatids exchange genetic material is known as
chiasma
synapsis
centromere
kinetochore
When homologous chromosomes pairs line up in metaphase I they do so at random. This is known as
Crossing Over
Segregation
Independent Assortment
Original Orientation
If an organism gametes contain 4 chromosomes, then how many combinations could be made based on independent assortment?
2
8
16
32
If an organism diploid cells contain 16 chromosomes, then how many combinations could be made based on independent assortment?
16
256
586
65,536
X-inactivation can only take place in
males
females
The X chromosome that undergoes inactivation is known as
Barr body
bad X
inactive X
active X
This refers to the number of chromosomes in a cell
ploidy
euploid
aneuploidy
polyploidy
If an organism has the correct number of chromosomes per cell they are
ploidy
euploid
aneuploidy
polyploidy
If an organism has the incorrect number of chromosomes per cell they are
ploidy
euploid
aneuploidy
polyploidy
If an organism has three or more sets of chromosomes per cell they are
ploidy
euploid
aneuploidy
polyploidy
This image is known as a
chromosome picture
karyotype
polyploidy
aneuploidy
This karyotype is of a
male
female
This karyotype is of a
male
female
If a gamete experiences the loss of a chromosome due to nondisjunction it is known as
eusomy
monosomy
disomy
trisomy
If a gamete experiences the gain of a chromosome due to nondisjunction it is known as
eusomy
monosomy
disomy
trisomy
This karyotype belongs to an individual that has
euploid cells
monosomy
trisomy
polyploidy
This karyotype belongs to an individual with
Down Syndrome
Turner Syndrome
Trisomy 21
Klinefelter Syndrome
This karyotype belongs to an individual with
Down Syndrome
Turner Syndrome
Trisomy 21
Klinefelter Syndrome
If an individual is aneuploidy and is said to have "XO" for their sex chromosomes they have
Down Syndrome
Turner Syndrome
Trisomy 21
Klinefelter Syndrome
If an individual is aneuploidy and is said to have "XXY" for their sex chromosomes they have
Down Syndrome
Turner Syndrome
Trisomy 21
Klinefelter Syndrome
When a chromosome segment breaks from the chromosome, reverses its orientation, and then reattaches in it's original position it is known as an
inversion
translocation
duplication
deletion
When a chromosome segment breaks from a chromosome and reattaches to a nonhomologous chromosome it is known as a
inversion
translocation
duplication
deletion
When a chromosome segment is copied it is known as a
inversion
translocation
duplication
deletion
When a chromosome segment is deleted it is known as a
inversion
translocation
duplication
deletion
Polyploidy is common in
animals
plants
bacteria
archea
Which life cycle is defined as the dominant stage being diploid
diploid-dominant
haploid-dominant
alteration of generations
Which life cycle is defined as the dominant stage being haploid
diploid-dominant
haploid-dominant
alteration of generations
Which life cycle has both stages apparent
diploid-dominant
haploid-dominant
alteration of generations
The science of heredity and variation in living organisms
gene
genetics
molecular genetics
mendelian genetics
The field of biology that studies the structure and function of genes at a molecular level
gene
genetics
molecular genetics
mendelian genetics
A set of basic principles relating to the transmission of hereditary characteristics from parent organisms to their children.
gene
genetics
molecular genetics
mendelian genetics
Who is the father of genetics?
James Watson
Francis Crick
Gregor Mendel
Charles Darwin
Mendel was praised during his time for his work with pea plants.
True
False
When characteristics can be seen as a range of small differences among indviduals ("blend" of parents")?
continuous variation
discontinuous variation
dominant-recessive traits
intermediate variation
When characteristics can be seen as one of two distinguishable trait)?
continuous variation
discontinuous variation
dominant-recessive traits
intermediate variation
Mendel experimented with
bacteria
garden pea plants
daphnia
drosophila
Select the advantages of using pea plants
controlled matings
true-breeding strains
observable traits with 2 distinct forms
only 3 characteristics can be seen
Mendel is the father of genetics becuase of his work we know:
genes are carried on chromosomes
chromosomes are the basic unit of heredity
chromosomes replicate, express, or mutate
homologous chromosomes code for different genes
Mendel studied how many characteristics of pea plants?
2
5
7
11
Which of the following are characteristic that were studied by Mendel?
seed shape
flower color
pod size
size of flower
Which generation consists of true-breeders that only produce one trait for a gene?
parental generation
first filial generation
second filial generation
Which generation consists of hybrid progeny that show only the dominant trait?
parental generation
first filial generation
second filial generation
Which generation consists of offspring from hybrid plants undergoing self-fertilization?
parental generation
first filial generation
second filial generation
Which of the following is NOT a hypothesis Medel came up with?
genes are found in alternative versions (alleles)
an organism inherits two alleles for each characteristic
in hybrids, the dominant allele determines the organism's appearance
in hybrids, the domninant and recessive allele appear
law of segregation
The physical expression of a trait
phenotype
genotype
allele
gene
The genetic makeup of an individual
phenotype
genotype
allele
gene
A unit of inheritance
phenotype
genotype
allele
gene
alternative form of a single gene
phenotype
genotype
allele
gene
When both alleles inherited are capital (S S)
homozygous dominant
heterozygous
homozygous recessive
When both alleles inherited are lowercase (s s)
homozygous dominant
heterozygous
homozygous recessive
When the alleles inherited are different (S s)
homozygous dominant
heterozygous
homozygous recessive
The predictive tool used to determine genotypic and phenotypic ratios of offspring
Mendel Rectangle
Punnett Square
Gregor Circle
Watson Triangle
Capital letters represent the ________________ trait.
dominant
recessive
Lowercase letters represent the ________________ trait.
dominant
recessive
Which Punnett Square cross is used to study one characteristic?
Dihybrid
Hybrid
Trihybrid
Monohybrid
Which Punnett Square cross is used to study two characteristic?
Dihybrid
Hybrid
Trihybrid
Monohybrid
In heterozygotes, one trait conceals the other trait it is which inheritance pattern?
dominant-recessive
incomplete dominance
co-dominance
multiple alleles
sex-linked
Heterozygous individuals show a blending of traits; it is which inheritance pattern?
dominant-recessive
incomplete dominance
co-dominance
multiple alleles
sex-linked
Heterozygous individuals show both traits; it is which inheritance pattern?
dominant-recessive
incomplete dominance
co-dominance
multiple alleles
sex-linked
When more than two alleles exist for a trait it is which inheritance pattern?
dominant-recessive
incomplete dominance
co-dominance
multiple alleles
sex-linked
Inheritance of traits that lie on sex chromosomes is which inheritance pattern?
dominant-recessive
incomplete dominance
co-dominance
multiple alleles
sex-linked
Inheritance of traits that are governed by more than one gene is which inheritance pattern?
epistasis
incomplete dominance
polygenic
multiple alleles
When one gene interferes with the expression of another gene it is which inheritance pattern?
epistasis
incomplete dominance
polygenic
multiple alleles
If genes are linked it violates the law of independent assortment.
true
false
When true breeding pea plants are crossed the offspring are all _____________.
homozygous dominant
heterozygous
homozygous recessive
In Mendel's studies of monohybrid crosses, when the F1 generation underwent self fertilization the offspring showed the following genotypic ratio?
1:1
1:2:1
3:1
2:2
In Mendel's studies of monohybrid crosses, when the F1 generation underwent self fertilization the offspring showed the following phenotypic ratio?
1:1
1:2:1
3:1
2:2
In pea plants, flowers that bud on the top of the plant (terminal position) is dominant, and flowers that bud on the sides of the plant (axial position) is recessive. Cross a heterozygous terminal flowering plant with a homozygous terminal flowering plant. Which of the following genotypes is seen in the offspring?
TT
Tt
tt
In pea plants, flowers that bud on the top of the plant (terminal position) is dominant, and flowers that bud on the sides of the plant (axial position) is recessive. Cross a heterozygous terminal flowering plant with a homozygous terminal flowering plant. Which of the following phenotypes is seen in the offspring?
terminal flowering plants
axial terminal plants
This can be used to determine whether an organism expressing the dominant trait is homozygous or heterozygous for the trait.
dominant test
test cross
Punnett Square
recessive test
When completing a test cross, one parent always has to be ____________________?
homozygous dominant
heterozygous
homozygous recessive
In Mendel's studies of dihybrid crosses, when the F1 generation underwent self fertilization the offspring showed the following phenotypic ratio?
8:8
7:4:4:1
9:3:3:1
3:1
Genes assort randomly because they are on different chromosomes which algin randomly at the metaphase plate, this is known as the
Principle of Dominance
Principle of Independent Assortment
Law of Segregation
Law of Randomness
Each gamete only gets ONE copy of each allele due to the separation of chromosomes during anaphase I, this is known as the
Principle of Dominance
Principle of Independent Assortment
Law of Segregation
Law of Randomness
What method can be used to determine the gametes of the parents in a dihybrid cross?
What gametes?
BOIL
FOIL
SOIL
A long neck yellow giraffe (TtYy), mates with a short neck orange giraffe (ttyy). What is the phenotype are seen in the offspring?
long neck and yellow
long neck and orange
short neck and yellow
short neck and orange
A individual will be called a __________ if they are heterozygous for a recessive disease.
carrier
homozygous dominant
homozygous recessive
lethal carrier
X-linked traits affect both males and females because they both will receive at least one X, but it affects females more because they get two.
True
False
Y-linked traits only affect males.
True
False
Males are considered ___________ because they only have one allele for any X-linked trait.
homozygous dominant
heterozygous
hemizygous
homozygous recessive
A woman who is a carrier for hemophilia marries a normal man. What is the genotypic ratio of the offspring?
1:1:1:1
2:2
3:1
1:1
A woman who is a carrier for hemophilia marries a normal man. What is the phenotypic ratio of the offspring?
2:1:1
2:2
3:1
1:1
In mice, coat color follows this expression Yellow (Y) and white (W) -colored mice are homozygous, while cream-colored mice are heterozygous (YW). This is known as
dominant-recessive
incomplete dominance
co-dominance
epistasis
In mice, coat color follows this expression Yellow (Y) and white (W) -colored mice are homozygous, while cream-colored mice are heterozygous (YW). If two cream-colored mice mate, what percentage of yellow mice are expected?
25%
50%
75%
0%
In mice, coat color follows this expression Yellow (Y) and white (W) -colored mice are homozygous, while cream-colored mice are heterozygous (YW). If two cream-colored mice mate, what percentage of cream mice are expected?
25%
50%
75%
0%
In mice, coat color follows this expression Yellow (Y) and white (W) -colored mice are homozygous, while cream-colored mice are heterozygous (YW). If two cream-colored mice mate, what percentage of white mice are expected?
25%
50%
75%
0%
In some chickens the allele for black coat is B and the allele for white coat is W. The heterozygous phenotype is known as erminette (black and white spotted). This is which type of inheritance?
dominant-recessive
incomplete dominance
co-dominance
epistasis
A black chicken and a white chicken are crossed. All offspring will be
black chickens
white chickens
erminette chickens
albino chickens
What are the two genotypes possible for a person who has A blood?
IAIA
IAi
IAIB
ii
What genotype is possible for a person who has O blood?
IAIA
IAi
IBi
ii
A woman with heterozygous type A blood is married to a heterozygous type B person, what proportion of their children will have A blood type?
0%
25%
50%
75%
A woman with heterozygous type A blood is married to a heterozygous type B person, what proportion of their children will have B blood type?
0%
25%
50%
75%
A woman with heterozygous type A blood is married to a heterozygous type B person, what proportion of their children will have AB blood type?
0%
25%
50%
75%
A woman with heterozygous type A blood is married to a heterozygous type B person, what proportion of their children will have O blood type?
0%
25%
50%
75%
A man with type AB blood is married to a woman with type O blood. They have two natural children and one adopted child. Jane has type A blood, Bobby has type B blood, and Grace has type O blood. Which child was adopted?
Jane
Bobby
Grace
None of them
Which of the following traits in humans show polygenic inheritance?
freckles
skin color
height
colorblindness
In cats, there is a gene which produces ticked fur (bands of different colors on each hair) called Agouti (H). The recessive allele (h) for this gene produces hair which is a solid color from end to end. In addition, there is a coat color gene which has a recessive albino allele (a) which, in the homozygote, prevents the production of any coat color pigment, resulting in a white cat with pink eyes, the traditional albino. This inheritance pattern is known as
dominant-recessive
incomplete dominance
co-dominance
epistasis
Which of the following scientists contributed to understanding the structure of DNA?
James Watson
Francis Crick
Maclyn McCarty
Rosalind Franklin
The condensed form of chromatin is known as ____________.
nucleosomes
chromsomes
chromatin
nucleotides
The double helix of DNA is made up of ____________________.
nucleosomes
chromsomes
chromatin
nucleotides
The double helix is wraped around _____________.
nucleosomes
chromsomes
chromatin
nucleotides
The uncondensed form of chromosomes is known as ____________.
nucleosomes
chromsomes
chromatin
nucleotides
The twisted molecule made up of two strands that contains hereditary information is known as ______________.
chromosome
chromatin
double helix
nucleotides
A nucleotide consists of the following:
phosphate
pentose sugar
nitrogenous base
hexose sugar
Which bases are purines?
adenine
thymine
guanine
cytosine
Which bases are pyrimidines?
adenine
thymine
guanine
cytosine
The strands of the double helix run in opposite directions this is known as _____________.
complementary base pairing
backwards ladder
antiparallel
reverse ladder
What type of bond is formed between bases?
nonpolar
ionic
covalent
hydrogen
What makes up the backbone of the double helix?
sugar
phosphate
adenine
guanine
What base always pairs with thymine?
adenine
thymine
guanine
cytosine
What base always pairs with cytosine?
adenine
thymine
guanine
cytosine
If a DNA sequence has the following: 5'ACTCCGAAT3'. What would be the complimentary strand?
3'TGAGGCTTA5'
5'TGAGGCTTA3'
5'CTGTTACCG3'
5'CTGTTACCG5'
Which sugar is found in RNA?
deoxyribose
ribose
Which sugar is found in DNA?
deoxyribose
ribose
Which of the following are bases found in DNA?
adenine
thymine
guanine
cytosine
uracil
Which of the following are bases found in RNA?
adenine
thymine
guanine
cytosine
uracil
Which of the following is double stranded?
DNA
mRNA
tRNA
rRNA
Which of the following is single stranded?
DNA
mRNA
tRNA
rRNA
Which of these is confined to the nucleus?
DNA
RNA
Which of these is not confined to the nucleus?
DNA
RNA
In prokaryotes, the entire genome is located on a single chromosome found in the _________ region of the cell.
nucleus
ribosomes
cytoplasm
nucleoid
When DNA is wrapped very tightly it is described as ______________?
supertightening
condensing
supercoiling
plasmids
Small pieces of non essential DNA commonly found in prokaryotes is known as ___________.
chromosomes
chromatin
nucleiod
plasmids
Eukaryotic DNA is separated from everything in the cell becuase it is housed in the __________.
ribosomes
cytoplasm
nucleus
nucleiod
Which stage of DNA replication is described as DNA polymerase adding complimentary base pairs to create a new strand?
Initiation
Elongation
Termination
Which stage of DNA replication is described as helicase unzipping the double helix?
Initiation
Elongation
Termination
Which stage of DNA replication is described as when two complementary strands are complete and bound together?
Initiation
Elongation
Termination
DNA replication is known as ___________________ becuase each new molecule consists of one original strand and one new strand.
conservative
semiconservative
dispersive
complementary
Which enzyme unzips DNA separating two stands?
helicase
ligase
DNA polymerase
topoisomerase
Which enzyme joins small fragments into a continuous chain?
helicase
ligase
DNA polymerase
topoisomerase
Which enzyme adds complementary nucleotides to the elongating chain?
helicase
ligase
DNA polymerase
topoisomerase
When DNA polymerase is able to continually add bases until the strand is complete it is known as the _________ strand?
Leading
Lagging
When DNA polymerase cannot continually add bases until the strand is complete it is known as the _________ strand?
Leading
Lagging
On the lagging strand, the pieces of nucleotides that are added are known as __________________.
Okazaki fragments
DNA segments
nucleotide fragments
polymerase segments
What is at the end of a DNA strand? It is a repitive sequence that repeats 100-1000 times, and helps to extend the life of a cell.
repeaters
telomeres
telomerase
primases
Telomeres allow for shortening of the DNA to take place without losing necessary genes.
True
False
Which enzyme replaces telomere as they are lost after DNA replication?
helicase
ligase
DNA polymerase
telomerase
DNA polymerase has the ability to proofread and replace bases as needed.
True
False
If DNA polymerase misses an incorrect base pair, then this mechanism is activated which allows enzymes to recognize incorrect bases and replace them.
nucleotide excision repair
mismatch repair mechanism
proofreading
transcription
To repair incorrect bases the DNA can be unwound and the strands unzipped, the incorrect base with be removed and then replaced by DNA polymerase, this repiar mechanism is known as _____________.
nucleotide excision repair
mismatch repair mechanism
proofreading
transcription
The central dogma describes how DNA is made from proteins.
True
False
When DNA is turned into mRNA, it is known as __________.
replication
transcription
translation
RNA synthesis
When mRNA is turned into a polypeptide chain, it is known as __________.
replication
transcription
translation
protein synthesis
Which processes takes place in the nucleus?
replication
transcription
translation
protein synthesis
Which processes takes place in the cytoplasm?
replication
transcription
translation
mRNA synthesis
Codons are
3 bases of DNA that code for mRNA
3 bases of mRNA that code for DNA
3 bases of mRNA that code for an amino acid
3 bases of DNA that code for an amino acid
Initiation, elongation, and termination are all steps for which process
replication
transcription
translation
When RNA polymerase binds to the promoter on DNA and causes it to unwind and unzip, it is which stage?
initiation
elongation
termination
translation
When RNA polymerase moves along the DNA making a complimentary mRNA strand, it is which stage?
initiation
elongation
termination
translation
When RNA polymerase encounters a terminator sequence, stops transcribing DNA, and releases immature mRNA, it is which stage?
initiation
elongation
termination
translation
RNA splicing removes _______ from the immature mRNA and joins ________ to produce a continuous mRNA molecule.
introns; exons
exons; introns
5' cap; poly-A tail
Poly-A tail; 5' cap
These are added to the mRNA moleucle to protect it when it enters the cytoplasm.
5' cap
introns
exons
poly-A tail
mRNA has to travel to the cytoplasm and meet up with a mitochondria to be tranlated.
True
False
_________ describes the specific sequence that determines which proteins are made and ultimately dictates structure and function of cells
codons
redundant
genetic code
unambiguous
When more than one codon gives you the same amino acid?
unambiguous
redundant
When any one codon codes for only one amino acid?
unambiguous
redundant
AUG codes for which amino acid?
Val
Met
Ile
Stop
UAA, UAG, and UGA code for which amino acid?
Val
Met
Ile
Stop
UUU code for which amino acid?
Val
Phe
Ile
Ser
CAA code for which amino acid?
Gln
His
Pro
Arg
Which of the followign RNAs is made by RNA polymerase from the DNA sequence?
mRNA
rRNA
tRNA
?RNA
Which of the followign RNAs makes up ribosomes?
mRNA
rRNA
tRNA
?RNA
Which of the following RNAs brings in amino acids and adds them to the growing polypeptide chain?
mRNA
rRNA
tRNA
?RNA
As tRNA molecules continue to add amino acids to a growing peptide chain and mRNA is read, it is which stage?
initiation
elongation
termination
tRNA is bound to a specific amino acid, what does a tRNA molecule have that matches up to a condon on mRNA?
amino acid
gene sequence
anticodon
codon
When mRNA attaches to the small subunit of a ribosome and is read until "AUG" is found which causes a tRNA and the large subunit to bind is which step of translation?
initiation
elongation
termination
The peptide chain continues to grow until a stop codon which leads to the dissociation of all machinery and the polypeptide chain?
initiation
elongation
termination
What is a change in the nucleotide sequence of DNA?
(a)
If a mutation is harmless it is known as a _________ mutation.
quiet
silent
nondescript
mutagen
All mutations are harmful.
True
False
Mutations can be spontaneous or induced by mutagens.
True
False
The ability to turn a gene "on" is known as
gene expression
gene promotion
gene communication
gene transcription
Prokaryotic gene regulation takes place at which levels
epigenetic
transcriptional
post-transcriptional
translational
post-translationsl
Eukaryotic gene regulation takes place at which levels
epigenetic
transcriptional
post-transcriptional
translational
post-translationsl
In prokaryotes, transcription and translation happen at the same time.
True
False
