Genetics Flashcards

(36 cards)

1
Q

What is the structure of DNA?

A

DNA is shaped in a double-helix form and made up of nucleotides which code for amino acids (Guanine, Cytosine, Thymine, Adenine), deoxyribose sugar, and a phosphate group.

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2
Q

What is the primary function of DNA?

A

It provides the code for all body proteins and our genetic material.

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3
Q

What does replication make?

A

DNA -> DNA

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4
Q

What does transcription make?

A

DNA -> mRNA

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5
Q

What does translation make?

A

mRNA -> polypeptide chain (protein); help of tRNA

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6
Q

What happens during DNA replication?

A

The DNA strand is untwisted and unzipped by helicase, DNA polymerase pairs complementary bases, adds new nucleotides, and proofs the new DNA strand.

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7
Q

DNA polymerase?

A

pairs complementary nucleotides and proof reads new DNA stand

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8
Q

What occurs during transcription?

A

RNA is synthesized from the DNA template with RNA polymerase, forming mRNA which moves out of the nucleus and into the cytoplasm.

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9
Q

RNA polymerase?

A

forms mRNA (functions like DNA polymerase)

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10
Q

What is the process of translation?

A

RNA directs the synthesis of a polypeptide via interaction with tRNA, which contains anticodons complementary to the mRNA codons.

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11
Q

What are euploid cells?

A

Cells that have multiples of the normal number of chromosomes.

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11
Q

ribosome?

A

joins mRNA and tRNA (carries base pairs) for protein synthesis

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12
Q

Define polyploidy.

A

A euploid cell that has more than the diploid number.

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13
Q

What is trisomy?

A

A cell containing 3 copies of one chromosome.

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14
Q

What is monosomy?

A

The presence of only one copy of any chromosome, typically lethal.

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15
Q

What is nondisjunction?

A

Failure of homologous chromosomes or sister chromatids to separate normally during mitosis or meiosis.

16
Q

What is Turner syndrome?

A

A condition characterized by having only one X chromosome.

17
Q

What is Klinefelter syndrome?

A

A condition characterized by the presence of an extra X chromosome (XXY).

18
Q

What is a deletion in chromosome structure alterations?

A

Chromosome breakage or loss of DNA.

19
Q

What is codominance?

A

A genetic scenario where both alleles are expressed.

20
Q

Define homozygous.

A

When genes are identical.

21
Q

Define heterozygous.

A

When genes are different.

22
Q

What is a karyotype?

A

An individual’s complete set of chromosomes.

23
Q

What is a genotype?

A

The specific set of alleles someone has.

24
What is a phenotype?
How the genotype gets expressed, resulting from interaction with the environment.
25
What is Cri du chat an example of?
deletion of chom. 5; not passed down
26
what is cystic fibrosis an example of?
autosomal recessive disorder
27
What is down syndrome an example of?
nondisjunction - trisomy 21
28
What is Duchenne muscular dystrophy an example of?
X-linked recessive
29
What is Huntington's disease an example of?
Autosomal dominant.
30
What is the difference between autosomal dominant and autosomal recessive disorders?
Autosomal dominant requires only one affected allele to express the disease; autosomal recessive requires two affected alleles.
31
What is penetrance?
The percentage of individuals with a specific genotype who express the expected phenotype.
32
What is expressivity?
The variation in a phenotype associated with a particular genotype.
33
What environmental factors influence hypertension?
Sodium intake, lack of exercise, stress, obesity.
34
What is the inheritance pattern of sex-linked disorders?
Usually expressed in males; affected males cannot pass to sons but can to daughters.
35
Are diseases multifactorial?
YES diabetes, hypertension, breast cancer. all have genetic and environmental components