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WorksheetsUnit 6 and 7
Total questions: 48
Worksheet time: 24mins
Place the components in order, from smallest to largest.
1. Chromosome
2. DNA nucleotide
3. Codon
4. Gene
1-2-4-3
2-3-4-1
3-4-2-1
4-3-2-1
A scientist is doing an experiment to identify different molecules. Some components of these are listed in this table. Which of the four molecules is DNA, based on the table to the right?
Molecule 1
Molecule 2
Molecule 3
Molecule 4
The main difference between the four nucleotides that make up DNA is that they have different ________.
sugars
uracil
phosphate
bases
in humans, where does DNA replication take place.
Cytoplasm
Nucleous
Ribosome
Vacuole
Use the diagram AND your knowledge of biology to answer this question. Structures 3 and 4 are held together by ____.
Weak peptide bonds
Strong hydrogen bonds
Weak hydrogen bonds
strong peptide bonds
The cellular process of creating two new DNA molecules from one original copy is called replication. WHich statement is the BEST description of this process?
DNA opens up and RNA copies it
DNA opens up and completely unwinds to make two new molecules
DNA opens up and each strand is used as a template for a new strand
RNA opens up the DNA and uses each strand as a template for a new strand
The diagram shown here represents a portion of a nucleic acid molecule. The part indicated by the arrow COULD be_____
Adenine
Uracil
Deoxyribose
Phosphate
Before a cell can divide, it must copy its DNA one ______ at a time in a process called DNA replication.
base
sugar
nucleotide
gene
Which of the following statements about the leading strand is true?
it is synthesized discontinuously and uses 1 RNA primer
It is synthesized discontinuously and uses multiple RNA primers
it is synthesized continuously and uses multiple RNA primers
it is synthesized continuously and uses 1 RNA primer
What is an example of a molecule produce by DNA replication
Glucose
Glycogen
A fatty acid
A polypeptide
in humans, WHERE does transcription take place
Nucleus
Cytoplasm
Ribosome
Rough ER
Which statement below BEST summarizes the role of DNA in cell?
It guides cell division
It protects cells from infection
It provides the instructions for making proteins
It regulates chemical processes that provide the cell with energy
During transcription, what does mRNA do?
It delivers DNA's instructions for making proteins
It constructs proteins out of amino acids
It strings together two complementary RNA strands
It strings together two complementary DNA strands.
Which of the following is an accurate description of the processes used to turn the DNA code of a gene into a protein?
Transfer RNA molecules carry the messenger RNA to the ribosome
Ribosomes go into the nucleus to read off the genes in the DNA
It takes one DNA base to code for three amino acids in a protein
Transfer RNA delivers specific amino acids to the ribosome, matching messenger RNA codons.
The sequence of ________ in a DNA molecule determines the protein that will be produced.
lipids
nucleotides
proteins
sugars
Two similar chromosomes that you inherit from your parents ( one from your mother and one from your father) are called?
Homologous chromosomes
Sister chromatids
Sex Chromosomes
Homologous alleles
Which event takes place during anaphase 2 of meiosis?
Nuclear membrane breaks down.
Sister chromatids separate
Homologous chromosomes
Cytoplasm divides
Which cells are NOT formed during meiosis?
Somatic cells
Gametes
Sex cells
Sperm cells
A sperm cell of an octopus has 14 chromosomes. What is the total number of chromosomes that should be present in a stomach cell of the same octopus?
7
14
28
46
Compared to the number of chromosomes contained in a body cell, how many chromosomes would normally be contained in a gamete
The same number
Twice as many
1/4th as many
Half as many
Both male and female gametes are created during the process of meiosis. The formation of male gametes or sperm is called spermatogenesis, there would _________ male gametes created that are all genetically ___________.
2; identical
2; unique
4; identical
4; unique
In which phase of meiosis would certain gene segments of the homologous pairs of chromosomes "crossover" and exchange genetic information?
Prophase 1
Metaphase 1
Anaphase 1
Telophase 1
Somatic cells in humans contain ________ chromosomes and an example is ______
30; skin cells
23; heart cells
46; liver cells
46; sperm cells
Which event takes place during the metaphase 1 of meiosis?
nuclear membrane breaks down
sister chromatids line up in middle of cell
cytoplasm divides
homologous chromosome pairs line up in middle of cell
The form of a gene that is always expressed if present is the _________form.
recessive
dominant
homologous
heterozygous
Which of Mendel's laws BEST explains why a heterozygous genotype will show a dominant phenotype?
Law of Dominance
Law of segregation
Law of Independent Assortment
Chromosome Theory of Inheritance
Two parents have the genotype Gg for a genetic disorder caused by a recessive allele. What is the chance that any of their children will inherit the disorder?
25%
50%
75%
100%
Which of Mendel's laws states that organisms inherit two copies of each gene and donate one copy to each of their offspring?
Law of Dominance
Law of segregation
Law of Independent Assortment
Chromosome Theory of Inheritance
In pigs, the allele for a wavy, rough coat (R) is dominant to the allele for a soft, fine coat (r). A rough coat boar and a soft coat sow mate. They produce several litters, 50% are rough smooth coat. What must be the genotypes of the parents to create this phenotype ratio.
Homozygous dominant and homozygous recessive
Heterozygous and homozygous recessive
Homozygous dominant and heterozygous
Both heterozygous
If two parents with dominant phenotypes produce an offspring with a recessive phenotype, then probably
one parent is heterozygous
only one parent is heterozygous
both parents are homozygous dominant
both parents are homozygous recessive
both parents are heterozygous.
Given a dihybrid cross for a plant, where P (purple) is dominant to p (white) and S (spherical seeds) is dominant to s (dented seeds), what is the predicted phenotypic ratios if two plants are mated that are both heterozygous for both traits?
1 purple, spherical: 1 purple, dented: 1 white, spherical: 1 white dented
8 purple, spherical: 8 purple, dented: 0 white, spherical: 0 white dented
9 purple, spherical: 3 purple, dented: 1 white, spherical: 3 white dented
9 purple, spherical: 3 purple, dented: 3 white, spherical: 1 white dented
for an XX female to express a recessive sex-linked trait, she must have____________.
a Y chromosome
one recessive allele
two recessive alleles
two dominant alleles
Human height occurs in a continuous range because it is affected by the interaction of many genes, making it a(n)
autosomal trait
sex-linked trait
polygenic trait
codominant trait
Red hair and freckles inherited together. Which of the following patterns of inheritance explains this?
linked genes
multiple alleles
Sex-Linked
Codominance
In a newly discovered species of flower, it was discovered that the color of the flowers is determined by two different genes. Which of the following inheritance patterns is this?
Multiple alleles
incomplete dominance
Linked genes
Polygenic inheritance
What is the MAIN reason that sexlinked disorders are most often observed in males?
The X chromosome only has genes for genetic disorders
The Y chromosome cannot have genes that cause genetic disorders
The Y chromosome cannot mask alleles on the X chromosome
The X chromosome has genes only for sex determination
Which chromosome shown to the right would be considered homologous?
A and B
B and C
A and C
D and E
In order for a mutation to be passed on from parent to offspring, the mutation must occur in
somatic cells.
gametes.
brain cells.
any cell of the body.
On a pedigree, how would a female individual with a disease be notated?
As a shaded circle
As an unshaded circle
As a shaded square
As an unshaded square
Tay Sach's disease is a fatal genetic condition in which affected individuals cannot breakdown fate properly. Children who inherit the disease rarely live past the age of five. The disease is cause by the presence of a homozygous recessive gene. If a child has Tay Sach's disease, what would her parents' genotypes have to be?
Her father is homozygous dominant; her mother homozygous recessive
Her father is heterozygous; her mother is homozygous dominant
Her father is homozygous dominant; her mother is homozygous dominant
Her father is heterozygous; her mother heterozygous
If a mutation only changes the nucleotide sequence for a single protein, then it is known as a
gene mutation.
chromosomal mutation
translocation
nondisjunction mutation
What kind of mutation occured in the sex chromosome of an individual with the genotype XXY?
Nucleotide deletion
Translocation
Nucleotide insertion
Nondisjunction
How would you categorize a genetic disorder that is equally likely in males and females and is caused by the presence of two affected alleles?
Autosomal recessive disorder
Sex-linked disorder
Autosomal dominant disorder
Sex chromosome disorder
When getting an X-ray taken at the doctor's office, you notice the technician cover you with a heavy vest. This vest, you are told, contains lead, a metal that can block X-rays, which are a form of radiation. THe technician covers your torso, and folds the vest over double across your reproductive organs (testes/ovaries). This is done because radiation can damage the DNA of these organs, causing a mutation you may pass to children. Substances like radiation and other certain chemicals are known as mutagens because
they causer cancer.
They cause mutations in the sequences of DNA.
they generate muteness
they damage proteins, which then changes the sequence of DNA.
Nondisjunction of autosomal chromosomes, such as chromosome 21, can result in which disorder?
Down syndrome
Klinefelter's syndrome
Turner's syndrome
Sickle-cell anemia
Selective breeding produces _________________.
more offspring
less offspring
transgenic offspring
desired traits in offspring
The goal of the Human Genome Project was to
create maps showing where genes are located on human chromosomes
create maps showing where genes are located on human genes
treat patients with genetic diseases
identify people with genetic diseases
A technique that allows engineers to artificially amplify a section of DNA by copying it over and over again in a lab is known as ______________.
Polymerase chain reaction
Personal genome sequencing
Recombinant DNA
Gene therapy
