Introduction to Genetics: Heredity and DNA (2024)

90 Questions

What is the backbone of DNA composed of?

Pentose sugar and phosphate group

Which scientist is credited with the discovery that the proportion of nitrogenous bases in DNA are equal?

Chargaff

What does a gene code for?

A segment of a DNA molecule that codes for a particular trait

What is the non-condensed form of genetic material known as?

Chromatin

What is the process of producing one individual that is genetically identical to another using a single cell or tissue?

Cloning

During which stage of the cell cycle does the DNA replicate?

S (Synthesis) Phase

What is the period between cell divisions, where the cell grows, DNA replicates, and the cell prepares for mitosis called?

Interphase

Which of the following represents the four phases of mitosis in correct order?

Prophase, Metaphase, Anaphase, Telophase

What is the process in which a cell divides its cytoplasm into two new identical daughter cells?

Cytokinesis

Which of the following is a potential downside of cloning?

Expensive production of cloned plants and animals

In the context of genetically modified organisms (GMOs), what does GMO stand for?

Genetically Modified Organism

What is cancer defined as?

A process where cells divide uncontrollably

DNA ______ BASE PAIRING: pairing of the nitrogenous base of one strand of DNA with the nitrogenous base of another strand You only need to know the nucleotide sequence for one strand

COMPLEMENTARY

DNA has a helix shape (Franklin, 1951)

3

The proportion of nitrogenous bases are equal. (Chargaff, 1940)

2

______: a segment of a DNA molecule that codes for a particular trait Found at a specific location on a chromosome

GENE

A chromosome is the condensed form of genetic material. It’s DNA wrapped tightly around small proteins Chromatin is the non-condensed or relaxed form of genetic material.

CHROMOSOME

GENETICS The study of heredity and the variation of inherited characteristics ______: the passing of traits from parents to offspring

HEREDITY

______ INFORMATION is contained in a molecule of DNA The modern DNA model has 3 parts: Composed of pentose sugar, a phosphate group and one of four nitrogenous bases (Levene, 1920)

GENETIC

A segment of a DNA molecule that codes for a particular trait Found at a specific location on a chromosome

GENE

The backbone of DNA is composed of phosphate group and pentose sugar. The nitrogenous bases pair up: ◦ Thymine-Adenine ◦ Cytosine-Guanine

BACKBONE

The location of a gene on a chromosome

LOCUS

______ Genetic information is contained in a molecule of ______ The modern ______ model has 3 parts: Composed of pentose sugar, a phosphate group and one of four nitrogenous bases (Levene, 1920)

DNA

During which stage of the cell cycle does the DNA replicate?

S (Synthesis) Phase

Which scientist is credited with the discovery that the proportion of nitrogenous bases in DNA are equal?

Erwin Chargaff

What is the process in which a cell divides its cytoplasm into two new identical daughter cells?

Cytokinesis

What is the period between cell divisions, where the cell grows, DNA replicates, and the cell prepares for mitosis called?

Interphase

Which of the following represents the four phases of mitosis in correct order?

Prophase, Metaphase, Anaphase, Telophase

What is the process of producing one individual that is genetically identical to another using a single cell or tissue?

Cloning

Which of the following is a potential downside of cloning?

Cloned plants and animals may be expensive

What does a gene code for?

A protein or RNA molecule

What is the non-condensed form of genetic material known as?

Chromatin

What is cancer defined as?

Occurs when cells divide uncontrollably

In the context of genetically modified organisms (GMOs), what does GMO stand for?

Genetically Modified Organisms

What is the backbone of DNA composed of?

Sugar-phosphate backbone

DNA has a ______ shape

helix

The location of a gene on a chromosome

locus

The backbone of DNA is composed of ______ group and pentose sugar

phosphate

What is the non-condensed form of genetic material known as?

chromatin

A segment of a DNA molecule that codes for a particular trait Found at a specific location on a chromosome

gene

GENETICS The study of heredity and the variation of inherited characteristics ______: the passing of traits from parents to offspring

heredity

What does a gene code for?

a particular trait

Carries information for hundreds or thousands of different genes

chromosome

What is cancer defined as?

uncontrolled cell growth

What is the process of producing one individual that is genetically identical to another using a single cell or tissue?

cloning

Which of the following represents the four phases of mitosis in correct order?

prophase, metaphase, anaphase, telophase

The proportion of nitrogenous bases are equal. (Chargaff, 1940)

DNA

Mitosis is the process by which a cell divides the genetic material in its nucleus into two identical nuclei. It is used for: Growth, Reproduction, Repair

mitosis

______ is the process in which a cell divides its cytoplasm into two new identical daughter cells. The same number and type of chromosomes in each cell

cytokinesis

The proportion of nitrogenous bases are equal. (Chargaff, 1940)

DNA

______ is the non-condensed form of genetic material known as

chromatin

The backbone of ______ is composed of phosphate group and pentose sugar. The nitrogenous bases pair up: Thymine-Adenine, Cytosine-Guanine

DNA

______ is the backbone of DNA composed of

phosphate group and pentose sugar

______ is the period between cell divisions, where the cell grows, DNA replicates, and the cell prepares for mitosis

interphase

______ is the modern DNA model has 3 parts: Composed of pentose sugar, a phosphate group and one of four nitrogenous bases (Levene, 1920)

DNA

______ Genetic information is contained in a molecule of ______ The modern ______ model has 3 parts: Composed of pentose sugar, a phosphate group and one of four nitrogenous bases (Levene, 1920)

DNA

The replication of chromosomes results in a pair of ______

sister chromatids

______ is the process of producing one individual that is genetically identical to another using a single cell or tissue

cloning

The passing of traits from parents to offspring

heredity

SEXUAL REPRODUCTION The production of offspring from the fusion of two sex cells ◻ Usually from two different parents ◻ The genetic makeup of the offspring is different from that of either parent

gametes

SOMATIC CELLS: cells that perform mitosis EXAMPLE: ◻ GAMETE CELLS: cells that perform meiosis EXAMPLE: ◻ ◻ skin cells sex cells

muscle

hom*oLOGOUS CHROMOSOMES ◻ ◻ Pairs of chromosomes that are similar in structure and carry similar genetic information You get one chromosome from your mother and one chromosome from your father

hom*ologous

DIPLOID NUMBER The number of chromosomes in somatic cells There are ______ chromosomes in a typical human somatic cell

46

HAPLOID NUMBER ◻ ◻ ◻ The number of chromosome in gamete cells The number of chromosomes in gamete cells is half the number of somatic cells There are ______ chromosomes in a typical human gamete cell

23

MEIOSIS ◻ ◻ ◻ ◻ A form of cell division in which the resulting daughter cells have half the number of chromosomes as the parent cell There are two stages: Meiosis I and Meiosis II Results in the formation of four gamete cells It takes place only in ______ tissue of sexually reproducing organisms

reproductive

MITOSIS VS.

meiosis

MEIOSIS ______

Variety is the Spice of Life.

FERTILIZATION: when two gamete cells combine to form a single ______ cell ZYGOTE: the first cell of a new individual

zygote

MEIOSIS STAGES OF MEIOSIS MEISOSIS I ◻ ◻ ◻ ◻ Prophase I Metaphase I Anaphase I Telophase I

Interphase

MEIOSIS II ◻ ◻ ◻ ◻ Prophase II Metaphase II Anaphase II Telophase II

Meiosis

TELOPHASE I ◻ ◻ The cells begin to divide Each daughter cell has only one member of each original pair

Cytokinesis

MEIOSIS II ◻ ◻ ◻ ◻ Begins immediately after Telophase I There is NO duplication of DNA between Meiosis I and Meiosis II The chromosomes still consist of sister chromatids, however, the sister chromatids are no longer identical Meiosis II continues on like Mitosis

Prophase II

SPERMATOGENESIS ◻ ◻ ◻ The production of sperm cells There is even division of the cytoplasm at each stage of meiosis The final product is four SPERM cells

Spermatids

NON-DISJUNCTION ◻ ◻ ◻ ◻ The separation of chromosomes occurs incorrectly It can happen during Meiosis I or Meiosis II It results in a cell that can contain too many or too few chromosomes If that cell is involved in fertilization, the zygote will have an abnormal number of chromosomes

Anaphase II

TRISOMY ◻ A chromosomal abnormality in which there are three hom*ologous chromosomes

Trisomy

DOWN SYNDROME ◻ ◻ An individual that has three copies of chromosome number 21 These individuals experience physical and mental challenges

Down Syndrome

TURNER SYNDROME ◻ ◻ An individual that has only one X chromosome These individuals are female in appearance but do not mature sexually and are sterile

Turner Syndrome

KLINEFELTER SYNDROME ◻ ◻ An individual with two X chromosomes and one Y chromosome These individuals are male in appearance with feminine body characteristics and are usually sterile

Klinefelter Syndrome

During PROPHASE I there is an event that occurs to ensure that you have genetic variability: RECOMBINATION: the exchanging of genetic information called CROSSING OVER

Recombination

METAPHASE I – Further Genetic Variation ◻ ◻ The tetrads migrate towards the centre of the cell and align across the middle of the cell randomly RANDOM ASSORTMENT: chromosomes that come from the father will not stay together nor will chromosomes that come from the mother (aka Independent Assortment)

Metaphase I

Match the following stages of meiosis with their descriptions:

Prophase I = Chromosomes come together in hom*ologous pairsMetaphase I = The tetrads migrate towards the centre of the cell and align across the middle of the cell randomlyAnaphase I = The hom*ologous chromosomes move to opposite poles of the cellTelophase I = The cells begin to divide and each daughter cell has only one member of each original pair

Match the following syndromes with their descriptions:

Turner Syndrome = An individual that has only one X chromosome, appears female but does not mature sexually and is sterileKlinefelter Syndrome = An individual with two X chromosomes and one Y chromosome, appears male with feminine body characteristics and is usually sterileGonadogenesis = The production of sperm cells, with even division of cytoplasm at each stage of meiosis, resulting in four sperm cellsOogenesis = The production of egg cells, with unequal division of cytoplasm at each stage of meiosis, resulting in a single ovum

Match the following genetic abnormalities with their descriptions:

Non-disjunction = The separation of chromosomes occurs incorrectly, resulting in a cell that can contain too many or too few chromosomesTrisomy = A chromosomal abnormality in which there are three hom*ologous chromosomesMonosomy = A chromosomal abnormality in which there is a single chromosomeDown Syndrome = An individual that has three copies of chromosome number 21 and experiences physical and mental challenges

Match the following terms with their definitions:

Somatic Cells = Cells that perform mitosisGamete Cells = Cells that perform meiosisFertilization = When two gamete cells combine to form a single zygote cellZygote = The first cell of a new individual

Match the following with their descriptions:

Meiosis = A form of cell division resulting in four gamete cellsDiploid Number = The number of chromosomes in somatic cellsHaploid Number = The number of chromosomes in gamete cellsFertilization = When two gamete cells combine to form a single zygote cell

Match the following with their characteristics:

hom*ologous Chromosomes = Pairs of chromosomes that are similar in structure and carry similar genetic informationMeiosis II = Begins immediately after Telophase IDNA = Has a helix shapeMitosis = Used for growth, reproduction, repair

Match the following with their functions:

Genetics = The study of heredity and the variation of inherited characteristicsNon-Disjunction = The separation of chromosomes occurs incorrectlyRecombination = The exchanging of genetic information called crossing overDNA Replication = Occurs during S phase of the cell cycle

Match the following with their associations:

Prophase I, Metaphase I, Anaphase I, Telophase I = Stages of Meiosis IThymine-Adenine, Cytosine-Guanine = DNA base pairingKlinefelter Syndrome = An individual with two X chromosomes and one Y chromosomeDown Syndrome = An individual that has three copies of chromosome number 21

Match the following with their characteristics:

Meiosis I, Meiosis II = Two stages of meiosisRandom Assortment = Chromosomes align across the middle of the cell randomlyTrisomy = A chromosomal abnormality in which there are three hom*ologous chromosomesGMO = Stands for Genetically Modified Organism

Test your knowledge on the basics of genetics including heredity, DNA structure, and key discoveries in the field.

Introduction to Genetics: Heredity and DNA (2024)

FAQs

Introduction to Genetics: Heredity and DNA? ›

Your chromosomes contain the blueprint for your body – your genes. Almost every cell in the human body contains a copy of this blueprint, mostly stored inside a special sac within the cell called the nucleus. Chromosomes are long strands of a chemical substance called deoxyribonucleic acid (DNA).

What is the introduction of genetic and heredity? ›

Genetics is termed as the study to understand the functioning of inheritance of traits from parents to offspring. The groundwork on which heredity stands is known as inheritance. It is defined as the procedure by which characteristics are handed down from one generation to the other.

What is genetics and DNA the science of heredity? ›

Genetics is the study of how heritable traits are transmitted from parents to offspring. Humans have long observed that traits tend to be similar in families. It wasn't until the mid-nineteenth century that larger implications of genetic inheritance began to be studied scientifically.

What is the study of heredity and DNA? ›

Genetics is the study of heredity. Gregor Mendel's work in the middle of the 19th century is where genetics got its start. Mendel had proposed that characteristics were passed down as distinct units of inheritance.

What are the basics of genetics and DNA? ›

DNA is made of 2 long, twisting molecules called the double helix. Chromosomes are packets of genes in a cell. Humans have 23 pairs (46 total). One member of each pair of chromosomes is inherited from the mother and the other from the father.

Why is DNA called heredity? ›

DNA is called hereditary material because it carries genetic information from one generation to the next.

What branch of science is genetics? ›

Genetics is the branch of biology concerned with the study of inheritance, including the interplay of genes, DNA variation and their interactions with environmental factors.

What does DNA stand for? ›

DNA stands for deoxyribonucleic (dee-OK-see-ri-bo-new-klee-ik) acid. It is the genetic information inside the cells of the body that helps make people who they are.

How is DNA passed down? ›

One copy is inherited from their mother (via the egg) and the other from their father (via the sperm). A sperm and an egg each contain one set of 23 chromosomes. When the sperm fertilises the egg, two copies of each chromosome are present (and therefore two copies of each gene), and so an embryo forms.

Where is DNA found in A cell? ›

Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA).

What are the 4 main things in DNA? ›

The information in DNA is stored as a code made up of four chemical bases: adenine (A), guanine (G), cytosine (C), and thymine (T). Human DNA consists of about 3 billion bases, and more than 99 percent of those bases are the same in all people.

What is DNA for beginners? ›

DNA or deoxyribonucleic acid is a molecule that contains the genetic code that is unique to every individual. Think of this code as an instruction manual for making all the proteins that form our bodies and help them thrive. The information coded in DNA is hereditary, meaning that it passes from parent to child.

What are the concepts of genetics and heredity? ›

Heredity describes how some traits are passed from parents to their children. The traits are expressed by genes, which are small sections of DNA that are coded for specific traits. Genes are found on chromosomes. Humans have two sets of 23 chromosomes— one set from each parent.

How do you write an introduction for genetics? ›

“Genetics” is the study of how traits are inherited. A trait is defined as a variation in the physical appearance of a heritable characteristic. It seeks to understand how traits are passed from generation to generation.

What is genetic heredity and why is it important? ›

All organisms inherit the genetic information specifying their structure and function from their parents. Likewise, all cells arise from preexisting cells, so the genetic material must be replicated and passed from parent to progeny cell at each cell division.

What is the meaning of genes and heredity? ›

Heredity refers to traits or characteristics that are passed down from parents to their children. Genetics more broadly refers to gene variations that may be inherited at conception or acquired later often due to environmental or lifestyle factors.

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