Brainscape's Knowledge GenomeTM

Browse over 1 million classes created by top students, professors, publishers, and experts.


See full index

Patho > Week 3: Genetics > Flashcards

Week 3: Genetics Flashcards

1
Q

What does DNA contain?

A

the basic genetic information in a cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Define nucleotide

A

molecules that contain a deoxyribose sugar, phosphate and a base

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the bases? How do they pair in complementary base pairing (include # of hydrogen bonds)?

A

Thymine, Cytosine, adenine, guanine

Adenine + Thymine: 2 hydrogen bonds
Guanine + Cytosine: 3 hydrogen bonds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How is single-stranded DNA formed?

A

formed between the sugars and phosphates of the nucleotides

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the sugar phosphate backbone?

A

structural framework of nucleic acids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q
  1. How is double-stranded DNA formed?

2. What is the ultimate structure double-stranded DNA forms?

A
  1. formed as hydrogen bonds form between bases between two strands of DNA
  2. double-helix
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How are DNA strands oriented?

A

5’ to 3’ orientation, strands are arranged in opposite directions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How is DNA organized in the nucleus and when is this structure visible in the cell?

A

Organized in chromosomes, visible during the cell cycle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How are histones used?

A

DNA is wrapped around histones to consolidate and organize the genetic information

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How is chromatin formed?

A

Chromatin formed when DNA associates with histones

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the genome?

A

the haploid set of chromosomes in a gamete or microorganism, or in each cell of a multicellular organism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is a karyotype?

A

evaluation of the number and content of chromosomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Where (1) and how (2) does DNA replication occur (3 main steps)?

A
  1. the nucleus
  2. DNA polymerase makes a copy of the genetic information in each chromosome
    - DNA replication begins at specific sites in the DNA and proceeds in a 5’ to 3’ direction
    - Molecule is unwound to create a replication fork where complementary base pairing is done by polymerase – base paring ensures DNA information is copied faithfully
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Define mitosis & cytokinesis

A

Mitosis: division of the nucleus
Cytokinesis: division of the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Explain the basic functions of DNA with regard to replication and translation

A

Replication: performed to maintain the genetic information in a cell
Translation: process by which RNA translates DNA into a form that can be used for protein synthesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Define semi-conservative replication (1) and explain the value of this process to health and disease (2)

A
  1. DNA is semi-conservative: each resulting DNA molecule contains one original strand and one newly synthesized strand
  2. Ensures mistakes or mutations can be fixed as the strand is marked with methyl groups that can be identified by DNA repair enzymes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

How does semi-conservative replication relate to DNA repair?

A

Using the methyl markings, DNA repair enzymes detect any mismatches between bases and fix the mistake in the new strand by using the original information as a template

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Describe what is meant by the term “genetic code” (1) and generally how a genetic mutation can alter protein structure and function (2)?

A
  1. Genetic code = groups of 3 nucleotides that specify an amino acid to be created
  2. Mutations can result in an aberrant protein sequence which can alter protein structure and function
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Define mutation, silent mutation, missense mutation, nonsense mutation.

A

mutation: errors in the DNA sequence

silent mutation: mutations that do not change the amino acid

missense mutation: mutation that alters the amino acid but may or may not alter protein structure and function

nonsense mutation: mutation that introduces a stop to protein synthesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

How is genetic information from DNA transferred through complementary base pairing?

A

Complementary base pairing between the mRNA codon and tRNA anticodon specify a strict association between the genetic information and amino acid sequence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Define and distinguish between somatic and germline mutations.

A

Mutations in germline cells (gametes) can be inherited whereas mutations in somatic cells are not inherited

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

How is human genetics used for disease diagnosis?

A

Genetic changes can be markers of disease – predict disease risk or likelihood of response to certain treatments

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Define mitosis and meiosis. What cells do they occur in?

A

mitosis: division of the nucleus in somatic cells
meiosis: division of the nucleus in gametes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the name of the type of division associated with meiosis?

A

reduction division

25
Q

How many chromosomes does a diploid cell have? A haploid cell? Which processes (mitosis or meiosis) creates a diploid cell or a haploid cell?

A

Diploid - 46 chromosomes, maintained by mitosis

Haploid - 23 chromosomes, maintained by meiosis

26
Q

Define sex chromosome

A

chromosomes that determine sex of the human – XX/XY

27
Q

Define autosome

A

all chromosomes except sex chromosomes

28
Q

Define homologues

A

sequences on chromosome pairs are similar, but not identical as one of each allele is inherited from each parent

29
Q

Define sister chromatids

A

copies of chromosomes made during cell replication

30
Q

Phases of mitosis (4)

A
  1. Prophase: Nuclear membrane dissolves and two copies of each chromosome (sister chromatids) attach at the centromere
  2. Metaphase: Chromosomes line up on the equatorial plane of the cell
  3. Anaphase: Sister chromatids separate and chromosomes are pulled apart
  4. Telophase: Nuclear membrane forms around the two sets of chromosomes
31
Q

Phases of meiosis (2)

A

Meiosis I: reduction division stage that results in the formation of two haploid cells per diploid cell, homologous chromosomes separate but sister chromatids remain together. Results in two individual cells with 23 chromosomes.

Meiosis II: further separate each of the sister chromatids to generate four cells – each contains a copy of 23 homologous chromosomes

32
Q

What happens more specifically during meiosis I? (5)

A
  1. Homologous chromosomes line up in the middle of the cell
  2. Separate to opposite sides of the cell
  3. Random shuffling of maternal and paternal chromosomes occurs
  4. Crossing over or exchange between homologous segments of the sister chromatids that make up each homologous chromosome occurs
  5. Results in genetic recombination, which ensures that genetic information in the offspring is unique
33
Q

How do two haploid cells create one diploid cell during fertilization?

A

Gametes fuse together during fertilization to form diploid zygote

34
Q

Define genotype and phenotype

A

Genotype: genetic makeup of an organism

Phenotype: observable characteristics of an organism produced by the interaction between genotype and environment

35
Q

Define allele, dominant allele, recessive allele, heterozygous and homozygous

A

Allele: alternatives for each trait
Dominant allele: variation that will produce a phenotype
Recessive allele: an allele that is masked phenotypically by a dominant allele
Homozygous: both gene copies are the same at a specific allele
Heterozygous: gene copies are different at a specific allele

36
Q

What would be the likelihood of parents who are heterozygous for an autosomal recessive trait (like cystic fibrosis) to have an affected child? A carrier child? A wild-type child?

A

Affected child: 25%
Carrier child: 50%
Wild-type child: 25%

37
Q

What tool can be used to determine likelihood of allele inheritance in offspring?

A

Punnett square

38
Q

What would be the likelihood of parents who are heterozygous for an autosomal dominant trait (like Huntington disease) to have an affected child? A carrier child? A wild-type child?

A

Affected child: 75%
Carrier child: 0%
Wild-type child: 25%

39
Q

Define Mendel’s first law of the principle of segregation

A

two members of a gene pair segregate from each other in the formation of the gametes
half of the gametes carries one allele; the other half carries the other allele

40
Q

Define Mendel’s second law of the principle of independent assortment

A

genes for different traits assort independently of one another in gamete production
Genes controlling different individual loci are not transmitted together to the progeny but rather are inherited independently of one another

41
Q

Define single-gene disorders

A

caused by mutations in individual genes, may be present on one or both alleles

42
Q

Define chromosomal disorders

A

caused by an excess or deficiency of genes contained within a whole chromosome or chromosomal segment

43
Q

Define multifactorial disorders

A

caused by a combination of variations in a number of genes that together produce or predispose an individual to a serious defect, often in concert with environmental factors

44
Q

Most genetic disorders associated with human disease are considered ______, ______ or ______.

A
  1. complex
  2. multifactorial
  3. polygenic
45
Q

Define mitochondrial disorders (1)
What is the inheritance pattern? (2)
What are the s/sx of mitochondrial disorders? (3)

A
  1. alterations in the mitochondrial genome
  2. inherited exclusively from mother to child
  3. can affect single organ or multiple organs depending on severity of the mutation – sx include poor growth, loss of muscle coordination, muscle weakness
46
Q

Define genomic imprinting

A

phenotype depends on whether mutation was obtained from the mother or father

47
Q

Define triple repeat patterns

A

mutations in genes that involve the expansion of three nucleotides, change is atypical if it is on the X chromosome

48
Q

What is the inheritance pattern for an autosomal recessive trait? (1)
Examples of diseases (2)

A

Parents must be heterozygous or homozygous recessive

Examples: Cystic fibrosis, sickle cell anemia

49
Q

What is the inheritance pattern for an autosomal dominant trait? (1)
Examples of diseases (2)

A

Parents can be heterozygous or homozygous dominant

Examples: Achondroplasia (dwarfism), Marfan syndrome (connective tissue defects)

50
Q

What is the inheritance pattern for an X-linked recessive trait? (1)
Examples of diseases (2)

A

Single-locus genetic disorder

Examples: Duchenne muscular dystrophy, hemophilia A

51
Q

Define polyploidy, aneuploidy.

Give an example of a disease associated with aneuploid

A

Polyploidy: complete sets of extra chromosomes

Aneuploid: chromosome number that is not 23
- Example: Down syndrome - Trisomy 21

52
Q

What kind of chromosomal abnormality can result from nondisjunction?

A

Aneuploid

53
Q

Define chromosome inversion, deletion and translocation.

What is an example of translocation?

A

Chromosomal inversion: segment of a chromosome is reversed

Chromosomal deletion: segment of a chromosome is removed

Chromosomal translocation: segment of a chromosome breaks off and switches with a segment from another
- Example: Philadelphia chromosome which can give rise to chronic myeloid leukemia

54
Q

Turner syndrome:
What is the chromosomal change?
What are the major s/sx?

A

absence of all or part of the X chromosome

Short stature and lack ovaries – lack of development of secondary sexual characteristics

55
Q

Klinefelter syndrome:
What is the chromosomal change?
What are the major s/sx?

A

one or more additional X chromosomes with a normal male composition (XY)

testicular dysgenesis, enlarged breasts, small testes, inability to produce sperm, typically see changes occur during puberty

56
Q

Marfan syndrome:
What is the patho?
Major s/sx?

A

Patho: mutation of FBN1 gene which encodes the CT protein fibrillin-1, a component of the ECM including formation and maintenance of elastic fibers. 75% of cases are inherited autosomal dominant, 25% arise from new mutation

S/sx: unusually tall with long limbs and digits, cardiovascular changes can be life threatening

57
Q

Hemophilia A:
What is the patho?
Major s/sx?
Treatment?

A

Patho: inherited X-linked recessive trait with the defective gene located on the X chromosome

S/sx: bleeding and easy bruising

Tx: replace factor VIII, desmopressin

58
Q

Down Syndrome:
What is the patho?
Major s/sx?

A

Patho: often due to nondisjunction and is associated with advanced maternal age

S/Sx: slower physical development, developmental delays

59
Q

DNA damage can also occur due to ______or exposure to ______and ______. _______ can often be repaired by ______.

A
  1. environmental exposures
  2. chemicals
  3. radiation
  4. mutations
  5. DNA repair mechanisms

Patho (14 decks)

Brainscape helps you reach your goals faster, through stronger study habits.
© 2024 Bold Learning Solutions. Terms and Conditions