122 Flashcards

(36 cards)

1
Q

Concept Card

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➢ Genes provide information for building proteins. They don’t however directly create proteins. The production of proteins is completed through two processes: transcription and translation.

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➢ Transcription and translation take the information in DNA and use it to produce proteins. Transcription uses a strand of DNA as a template to build a molecule called RNA.

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➢ The RNA molecule is the link between DNA and the production of proteins. During translation, the RNA molecule created in the transcription process delivers information from the DNA to the protein-building machines. 1/16/2025 2

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5
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➢ Each strand of the DNA double helix contains a sequence of nucleotides that is exactly complementary to the nucleotide sequence of its partner strand. Each strand can therefore act as a template, or mold, for the synthesis of a new complementary strand (Figure 6–2). In other words, if we designate the two DNA strands as S and S, strand S can serve as a template for making a new strand S, while strand S` can serve as a template for making a new strand S (Figure 6–3).

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6
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➢ Thus, the genetic information in DNA can be accurately copied by the beautifully simple process in which strand S separates from strand S`, and each separated strand then serves as a template for the production of a new complementary partner strand that is identical to its former partner.

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7
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➢ DNA replication produces two complete double helices from the original DNA molecule, each new DNA helix identical (except for rare copying errors) in nucleotide sequence to the parental DNA double helix. 1/16/2025 6 Figure 6–3 DNA acts as a template for its own duplication. Because Figure 6–2 A DNA strand can serve as a the nucleotide A will successfully pair only with T, and G with C, each template. Preferential binding occurs between strand of DNA in the double helix—labeled here as the S strand and its pairs of nucleotides (A with T, and G with C) that complementary S’ strand—can serve as a template to specify the can form base pairs. This enables each strand to sequence of nucleotides in its complementary strand. In this way, act as a template for forming its complementary double-helical DNA can be copied precisely. Keep in mind that although strand. they are colored differently here, the template strands (orange) and the new strands (red) are chemically identical. Page 173 1/16/2025 7

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8
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➢ The DNA double helix is normally very stable: the two DNA strands are locked together firmly by the hydrogen bonds formed between the bases on each strand. To begin DNA replication, the double helix must first be opened up and the two strands separated to expose unpaired bases. As we shall see, the process of DNA replication is begun by special initiator proteins that bind to double-stranded DNA and pry the two strands apart, breaking the hydrogen bonds between the bases.

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9
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➢ The positions at which the DNA helix is first opened are called replication origins. In simple cells like those of bacteria or yeast, origins are specified by DNA sequences several hundred nucleotide pairs in length. This DNA contains both short sequences that attract initiator proteins and stretches of DNA that are especially easy to open. There is an A-T base pair held together by fewer hydrogen bonds than is a G-C base pair. Therefore, DNA rich in A-T base pairs is relatively easy to pull apart, and regions of DNA enriched in A-T base pairs are typically found at replication origins. 1/16/2025 8 Stages of DNA replication DNA replication can be thought of in three stages: initiation, elongation and termination 1) Initiation

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10
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➢ DNA synthesis is initiated at particular points within the DNA strand known as ‘origins’, which have specific coding regions. These origins are targeted by initiator proteins, which go on to recruit more proteins that help aid the replication process, forming a replication complex around the DNA origin. Multiple origin sites exist within the DNA’s structure; when replication of DNA begins, these sites are referred to as replication forks.

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11
Q

➢ Within the replication complex is the DNA helicase. This enzyme unwinds the double helix and exposes each of the two strands so that they can be used as a template for replication. It does this by hydrolyzing the ATP used to form the bonds between the nucleobases, thereby breaking the bond holding the two strands together.

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12
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➢ DNA primase is another enzyme that is important in DNA replication. It synthesizes a small RNA primer, which acts as a ‘kick-starter’ for DNA polymerase. This enzyme is ultimately responsible for the creation and expansion of new strands of DNA. 1/16/2025 11 Stages of DNA replication 2) Elongation

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13
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➢ Once DNA Polymerase has attached to the two unzipped strands of DNA (i.e. the template strands), it is able to start synthesizing new strands of DNA to match the templates. DNA polymerase is only able to extend the primer by adding free nucleotides to the 3’ end.

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14
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➢ One of the template strands is read in a 3’ to 5’ direction, therefore the new strand will be formed in a 5’ to 3’ direction. This newly formed strand is referred to as the leading strand. Along the leading strand, DNA primase only needs to synthesize an RNA primer once, at the beginning, to initiate DNA polymerase. This is because DNA polymerase is able to extend the new DNA strand by reading the template 3′ to 5′, synthesizing in a 5′ to 3′ direction as noted above.

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15
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➢ However, the other template strand (the lagging strand) is antiparallel and is therefore read in a 5’ to 3’ direction. Continuous DNA synthesis, as in the leading strand, would need to be in the 3′ to 5′ direction, which is impossible as DNA polymerase cannot add bases to the 5′ end. Instead, as the helix unwinds, RNA primers are added to the newly exposed bases on the lagging strand and DNA synthesis occurs in fragments, but still in the 5′ to 3′ direction as before. 1/16/2025 These fragments are known as Okazaki fragments. 12 Stages of DNA replication 3) Termination

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16
Q

➢ The process of expanding the new DNA strands continues until there is either no more DNA template strand left to replicate (i.e. at the end of the chromosome) or two replication forks meet and subsequently terminate. The meeting of two replication forks is not regulated and happens randomly along the course of the chromosome.

17
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➢ Once DNA synthesis has finished, the newly synthesized strands are bound and stabilized. For the lagging strand, two enzymes are needed to achieve this stabilization: RNAase H removes the RNA primer at the beginning of each Okazaki fragment, and DNA ligase joins these fragments together to create one complete strand. 1/16/2025 13 RNA polymerase is the enzyme responsible for making mRNA copies of genes Figure 7–6 Transcription produces an RNA complementary to one strand of DNA. The nontemplate strand of the DNA (the top strand in this example) is sometimes called the coding strand because its sequence is equivalent to the RNA product Page 352 1/16/2025 15 Translation is the process by which the genetic code contained within a messenger RNA (mRNA) molecule is decoded to produce a specific sequence of amino acids in a polypeptide chain.

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➢ It occurs in the cytoplasm following DNA transcription and, like transcription, has three stages: initiation, elongation, and termination. In this article, we will discuss the components and stages of DNA translation. Components of Translation

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➢ The key components required for translation are mRNA, ribosomes, and transfer RNA (tRNA).

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➢ During translation, mRNA nucleotide bases are read as codons of three bases. Each codon codes for a particular amino acid.

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➢ Every tRNA molecule possesses an anticodon that is complementary to the mRNA codon, and at the opposite end lies the attached amino acid. tRNA molecules are therefore responsible for bringing amino acids to the ribosome in the correct order, ready for polypeptide assembly. Page 247 1/16/2025 16

22
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➢ A single amino acid may be coded for by more than one codon. There are also specific codons that signal the start and the end of translation.

23
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➢ Aminoacyl-tRNA synthetases are enzymes that link amino acids to their corresponding tRNA molecules. The resulting complex is charged and is referred to as an aminoacyl-tRNA. 1) Initiation

24
Q

➢ For translation to begin, the start codon (5’AUG) must be recognized. This codon is specific to the amino acid methionine, which is nearly always the first amino acid in a polypeptide chain.

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➢ At the 5’ cap of mRNA, the small 40s subunit of the ribosome binds. Subsequently, the larger 60s subunit binds to complete the initiation complex. The next step (elongation) can now commence. Page 247 1/16/2025 17 2) Elongation
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➢ The ribosome has two tRNA binding sites; the P site which holds the peptide chain and the A site which accepts the tRNA.
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➢ While Methionine-tRNA occupies the P site, the aminoacyl-tRNA that is complementary to the next codon binds to the A site, using energy yielded from the hydrolysis of GTP.
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➢ Methionine moves from the P site to the A site to bond to a new amino acid there, starting the growth of the peptide. The tRNA molecule in the P site no longer has an attached amino acid, so leaves the ribosome.
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➢ The ribosome then translocates along the mRNA molecule to the next codon, again using energy yielded from the hydrolysis of GTP. Now, the growing peptide lies at the P site and the A site is open for the binding of the next aminoacyl-tRNA, and the cycle continues.
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➢ The polypeptide chain is built up in the direction from the N terminal (methionine) to the C terminal (the final amino acid). Page 247 1/16/2025 18 3) Termination
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➢ One of the three stop codons enters the A site. No tRNA molecules bind to these codons, so the peptide and tRNA in the P site become hydrolyzed, therefore releasing the polypeptide into the cytoplasm. The small and large subunits of the ribosome then dissociate, ready for the next round of translation. Page 247 1/16/2025 19 Figure 7–24 The nucleotide sequence of an mRNA is translated into the amino acid sequence of a protein via the genetic code. All the three-nucleotide codons that specify a given amino acid are listed above that amino acid, which is given in both its three-letter and one-letter abbreviations (see Panel 2–5, pp. 72–73, for the full name of each amino acid and its structure). By convention, codons are always written with the 5`-terminal nucleotide to the left. Note that most amino acids are represented by more than one codon, and that there are some regularities in the set of codons that specify each amino acid. Codons for the same amino acid tend to contain the same nucleotides at the first and second positions and to vary at the third position. There are three codons that do not specify any amino acid but act as termination sites (stop codons), signaling the end of the protein-coding sequence. One codon—AUG—acts both as an initiation codon, signaling the start of a protein- coding message, and as the codon that specifies methionine. Page 247 1/16/2025 20 Figure 7–23 Procaryotes and eucaryotes handle their RNA transcripts differently. (A) In eucaryotic cells, the initial RNA molecule produced by transcription contains both intron and exon sequences. Its two ends are modified, and the introns are removed by an enzymatically catalyzed RNA splicing reaction. The resulting mRNA is then transported from the nucleus to the cytoplasm, where it is translated into protein. Although these steps are depicted as occurring one at a time, in a sequence, in reality they occur simultaneously. For example, the RNA cap is usually added and splicing often begins before the transcript has been completed. Because of this coupling, transcripts of the entire gene (including all introns and exons) do not typically exist in the cell. Page 245 1/16/2025 21 Main Difference between Codon and Anticodon
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➢ Codon and anticodon are nucleotide triplets which specify a particular amino acid in a polypeptide. A specific rule set exists for the storage of genetic information as a nucleotide sequence either on DNA or mRNA molecules in order to synthesize proteins. That specific rule set is referred to as the genetic code. Codon is a group of three nucleotides, especially on the mRNA. Anticodon is present on tRNA molecules.
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➢ The main difference between codon and anticodon is that codon is the language which represents an amino acid on mRNA molecules whereas anticodon is the complement nucleotide sequence of the codon on tRNA molecules. Codon is a sequence of three nucleotides which specifies one amino acid in the polypeptide chain. Every gene that encodes a specific protein consists of a sequence of nucleotides, which represent the amino acid sequence of that particular protein. Genes utilize a universal language, the genetic code, in order to store the amino acid sequences of proteins. Genetic code consists of nucleotide triplets which are called codons. For example, the codon TCT represents the amino acid serine. Sixty-one codons can be identified in order to specify the twenty essential amino acids required by the translation. 1/16/2025 22 Anticodon
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➢ The three-nucleotide sequence on the tRNA, which is complementary to the codon sequence on the mRNA is referred to as the anticodon.
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➢ During translation, anticodon is complementary base paired with the codon via hydrogen bonding.
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➢ Therefore, each codon contains a matching anticodon on distinct tRNA molecules. The complementary base pairing of anticodon with its codon is shown in figure 4. 1/16/2025 23 Codon Anticodon Location Codon is located on the mRNA molecule Anticodon is located on the tRNA molecule Complementary Codon is complementary to the nucleotide Anticodon is complementary to the codon Nature triplet in the DNA Continuity Codon is sequentially present on the Anticodon is individually present on tRNAs mRNA Function Codon determines the position of the Anticodon brings the specified amino acid by amino acid the codon 1/16/2025 24