M6 Subtopic 2 Flashcards

1
Q

DNA stands for

A

Deoxyribonucleic Acid

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2
Q

molecule that carries the genetic instructions for life

A

DNA

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3
Q

It is made up of nucleotides (4)

A

Adenine, Thymine, Cytosine, Guanine

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4
Q

Who first discovered the Double Helix structure?

A

James Watson and Francis Crick in 1953,

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5
Q

DNA is composed of two long strands that coil around each other to form a ________

A

Double Helix

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6
Q

Each strand of DNA is made up of repeating units called…?

A

Nucleotides

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7
Q

Each nucleotide consists of three components:

A

A phosphate group
A sugar molecule (deoxyribose)
A nitrogenous base

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8
Q

The two strands of the DNA double helix are _____________, meaning the sequence of bases on one strand determines the sequence on the other

A

Complementary

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9
Q

Pairing of the nucleotides?

A

Adenine - Thymine / Uracil (RNA)
Cytosine - Guanine

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10
Q

describes the flow of genetic information from DNA to RNA to protein.

A

central dogma of molecular biology

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11
Q

process by which a cell copies its entire genome before cell division, ensuring that each daughter cell receives an identical set of genetic instructions

A

DNA replication

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12
Q

Steps of DNA replication, transcription, and translation.

A

Initiation
Elongation
Termination

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13
Q

begins at specific sites on the DNA molecule called origins of replication. Enzymes like helicase unwind the DNA double helix, creating replication forks

A

Initiation (replication)

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14
Q

DNA polymerase, the enzyme responsible for synthesizing new DNA strands, adds nucleotides to the exposed DNA template strands in a complementary fashion (A-T, C-G). On the leading strand, DNA is synthesized continuously, while on the lagging strand, it is synthesized in short fragments.

A

Elongation (replication)

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15
Q

In elongation, on the lagging strand, it is synthesized in short fragments called?

A

Okazaki fragments

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16
Q

It continues until the entire molecule has been copied. Enzymes like ligase seal the gaps between the Okazaki fragments, creating a continuous strand. The result is two identical DNA molecules, each with one old strand and one newly synthesized strand (semi-conservative replication).

A

Termination (replication)

17
Q

the process by which the information encoded in a gene’s DNA sequence is transcribed into messenger RNA (mRNA).

A

Transcription

18
Q

Where does transcription take place for eukaryotic and prokaryotic cells?

A

Nucleus (Eukaryotic)
Cytoplasm (Prokaryotic)

19
Q

RNA polymerase binds to a specific region of the DNA called the promoter, signaling the start of this process.

A

Initiation (transcription)

20
Q

RNA polymerase unzips the DNA and adds complementary RNA nucleotides to form an mRNA strand

A

Elongation (transcription)

21
Q

It ends when RNA polymerase reaches a terminator sequence, releasing the newly formed mRNA.

A

Termination (transcription)

22
Q

The process by which the genetic code carried by mRNA is decoded by ribosomes to synthesize a specific protein.

A

Translation

23
Q

Where does translation occur in both eukaryotic and prokaryotic cells?

24
Q

The ribosome assembles around the mRNA, and the first tRNA (transfer RNA) binds to the start codon (AUG) on the mRNA

A

Initiation (Translation)

25
The ribosome moves along the mRNA, reading each codon and bringing in the corresponding tRNA with its attached amino acid. The amino acids are linked together to form a polypeptide chain
Elongation (Translation)
26
When the ribosome reaches a stop codon (UAA, UAG, or UGA), the translation process ends, and the newly synthesized protein is released.
Termination (Translation)
27
the process by which the instructions in a gene are used to synthesize a functional product, typically a protein.
Gene expression
28
Eye color is determined by the amount and type of pigment present in the iris. What is this pigment called?
Melanin
29
Types of Mutations
Silent Missense Nonsense Frameshift
30
These mutations change a nucleotide without altering the amino acid sequence of the protein, usually having no effect on the protein's function
Silent Mutation
31
These mutations result in a different amino acid being incorporated into the protein, which may affect the protein's function, depending on the importance of the altered amino acid.
Missense Mutation
32
These mutations introduce a premature stop codon, leading to the production of a truncated, usually nonfunctional protein.
Nonsense Mutation
33
Insertions or deletions that shift the reading frame can result in a completely different and often nonfunctional protein.
Frameshift Mutation
34
Specific sequences of nucleotides within the DNA that encode instructions for building proteins that carry out most functions in a cell.
Genes
35
The entire set of genetic material in an organism
Genome