Unit 3: Flashcards

1
Q

Who discovered the chemical structure of DNA?

A

James Watson and Francis crick

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2
Q

What name is given to the structure of DNA?

A

Deoxyribonucleic

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3
Q

Four nitrogenous bases in DNA:

A
  1. Thymine
  2. Cytosine
  3. Adenine
  4. Guanine
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4
Q

What is complimentary base pairing?

A

Nucleutoid bases linked by an H bond. Guanine and cytosine are complimentary + adenine and thymine

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5
Q

3 components of a nucleotide:

A

Sugar (deoxyribose), a phosphate, and one of four bases (thymine, cytosine, guanine, adenine)

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6
Q

Tay Sachs: and what is the treatment?

A

Caused by absence of hex-a (vital enzyme). No cure but treatments are available for symptom care. (Seizures, epilepsy, mucus buildup, physical care, feeding tubes)

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7
Q

PKU:

A

Phenylketonuria. A rare genetic condition that causes amino acid (

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8
Q

PKU treatment:

A

Special diet that limits food with phenylalanine or high protein. Babies need special formula called lofenalac.

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9
Q

Sickle cell anemia:

A

The body produces abnormally shaped red blood cells (crescent or sickle shaped). They can block blood flow and cause clotting.

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10
Q

Karyotype:

A

Representation of The number, size, shape of chromosomes in organism

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11
Q

What can be learned from a karyotype?

A

It is easy to view abnormalities in the chromosomes (trisomy, missing chromosomes, mutations) that can cause problems in growth and development

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12
Q

Polygenic traits:

A

Characteristic controlled by 2 or more genes located on different areas on different chromosomes. (Controlled by atleast 3 genes

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13
Q

Traits are polygenic when:

A

When there is A wide variation in the trait

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14
Q

How is a DNA fingerprint made?

A

Obtain cells (skin, hair, blood). DNA is extracted and purified and sequences using gel electrophoresis. (- charge is applied so proteins move towards + charge). Compared to sample

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15
Q

What things can be cloned?

A

Plants, food, animals, body parts, drug production (animal proteins). To improve certain parts of something & to regrow human parts + medicine use

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16
Q

Pedigree:

A

The recorded ancestry showing genealogy.

17
Q

Four changes in chromosome structure:

A

Deletion, duplication, inversion, translocation

18
Q

Deletion:

A

Mutation where part of chromosome or DNA is lost during replication

19
Q

Duplication;

A

Duplication of a region of DNA that contains a gene

20
Q

Inversion:

A

Chromosome rearrangement where a segment of a chromosome is reduced end to end

21
Q

When does inversion occur::

A

When a single chromosome undergoes a breakage and rearrangement within itself

22
Q

Translocation:

A

Chromosomal segment is moved from one position to another (within the same Or to another chromosome)

23
Q

Amniocentesis:

A

Medical procedure where small amniotic fluid is sampled. used in prenatal diagnosis of chromosomal abnormalities. (Fetal infection and sex determination)

24
Q

Ultra sound:

A

Medical imaging technique that uses sound waves to produce picture inside the body.

25
Chorionic villus sampling:
Prenatal diagnosis to determine chromosomal or genetic disorders in fetus by taking a small sample of cells from the placenta
26
Fetoscopy:
Endoscopic procedure during pregnancy to allow access to fetus to the amniotic cavity, umbilical cord, and placenta
27
Law of segregation
During production of gametes, 2 copies of each hereditary factors separate so offspring aqquire one factor from each parent
28
Principle of dominance:
when individuals with contrasting traits are crossed, the offspring will have the dominant trait
29
Monohybrid cross:
Different variations of a trait for one genetic chromosome of interest
30
Dihybrid cross;
Cross between two different lines that differ in two observed traits
31
Incomplete dominance:
Blending of dominant and recessive (pink Roses)
32
Co dominance:
When alleles of heterozygote are fully expressed (Dalmatian)
33
Law of assortment:
Alleles separate independently during formation of gametes. Traits are transmitted independently to offspring
34
Somatic cell:
Any cell BUT REPRODUCTIVE
35
Cytokinesis
Physical process of cell division that divides the cytoplasm into 2 daughter cells
36
Haploid:
Single set of unpaired chromosomes
37
Meiosis:
Specialized cell division that reduces the chromosome number by half (creating four haploid cells distinct from the parent cell)
38
Random assortment:
the process where chromosome pairs align themselves at the middle of the cell
39
Mutations:
Change or mistake made in gene sequence