M6 Subtopic 2 Flashcards

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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 transcription.

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

Transcription 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?

A

Cytoplasm

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
Q

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

A

Elongation (Translation)

26
Q

When the ribosome reaches a stop codon (UAA, UAG, or UGA), the translation process ends, and the newly synthesized protein is released.

A

Termination (Translation)

27
Q

the process by which the instructions in a gene are used to synthesize a functional product, typically a protein.

A

Gene expression

28
Q

Eye color is determined by the amount and type of pigment present in the iris.

What is this pigment called?

A

Melanin

29
Q

Types of Mutations

A

Silent
Missense
Nonsense
Frameshift

30
Q

These mutations change a nucleotide without altering the amino acid sequence of the protein, usually having no effect on the protein’s function

A

Silent Mutation

31
Q

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.

A

Missense Mutation

32
Q

These mutations introduce a premature stop codon, leading to the production of a truncated, usually nonfunctional protein.

A

Nonsense Mutation

33
Q

Insertions or deletions that shift the reading frame can result in a completely different and often nonfunctional protein.

A

Frameshift Mutation