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159 Cards in this Set
- Front
- Back
An individual section of a DNA strand carrying the information needed for the synthesis of a specific protein. The basic unit of heredity. |
gene |
|
A subcellular particle that serves as the site of protein synthesis. |
ribosome |
|
The conversion of the code carried by mRNA into an amino acid sequence of a protein. |
translation |
|
A segment of DNA that carries no codes for amino acids. |
intron |
|
Circular, double-stranded DNA found in the cytoplasm of bacterial cells. |
plasmid |
|
The transfer of genetic information from a DNA molecule to a molecule of mRNA. |
transcription |
|
Movement of a ribosome along an mRNA during protein synthesis. |
translocation |
|
During the synthesis of RNA, an adenine nucleotide on DNA will be base-paired with |
uracil |
|
Which of the following is NOT a component of the site of protein synthesis? a.mRNA b.tRNA c.rRNA d.hnRNA e.more than one choice is correct |
hnRNA |
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The site on a tRNA molecule that bonds with an mRNA molecule is the |
anticodon |
|
Okazaki fragments are linked together by a |
ligase |
|
One strand of DNA has the base sequence AATGCT (written in the 5' to 3' direction). What is the base sequence for the complementary DNA strand in the 5' to 3' direction? a.AGCAUU b.CCGTAG c.GATGCC d.TTACGA e.AGCATT |
AGCATT |
|
During replication, nucleotides are joined together under the influence of .---blank.. |
DNA polymerase |
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How many nucleotide bases on an mRNA strand are needed to code for a peptide that is 8 amino acids in length? |
24 |
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The central dogma of molecular biology involves |
DNA → RNA → protein |
|
mRNA in eukaryotic cells contains information from which DNA segments when the transcription is complete? |
exons only |
|
The fact that most amino acids are represented by more than one mRNA codon is referred to as |
degeneracy |
|
An RNA chain being synthesized grows in the ________ direction. |
5' → 3' |
|
What stage of protein synthesis is occurring when the large and small ribosomal units move one codon at a time along the mRNA strand? |
chain elongation |
|
In genetic engineering, desirable DNA can be cleaved at specific base sequences by |
restriction enzymes |
|
Nucleic acids are classified into two categories: .---blank., found mainly in the cytoplasm of living cells, and .---blank., found primarily in the nuclei of cells. |
ribonucleic acid (RNA) deoxyribonucleic acid (DNA) |
|
.---blank.is the nucleic acid found primarily in the cytoplasm of living cells. |
ribonucleic acid (RNA) |
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Both DNA and RNA are polymers, consisting of long, linear molecules. The repeating structural units, or monomers, of the nucleic acids are called .---blank.. |
nucleotides |
|
The repeating units, or monomers, found in DNA and RNA are called .---blank.. |
nucleotides |
|
Nucleotides are composed of three components: a .---blank., a sugar, and a phosphate |
heterocyclic base |
|
Three components: a heterocylic base, a .---blank., and a phosphate comprise all nucleotides. |
sugar |
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.---blank. commonly found in nucleic acids can be classified as either a pyrimidine or a purine. |
Heterocyclic bases |
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The heterocyclic base portions of nucleic acids are either .---blank. or purines. |
pyrimidines or purine |
|
The three .---blank. bases are uracil, thymine, and cytosine, usually abbreviated U, T, and C. Adenine (A) and guanine (G) are the two purine bases |
pyrimidine |
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A and G are .---blank. bases. |
purine |
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Adenine, guanine, and cytosine are found in both DNA and RNA, but .---blank.is ordinarily found only in RNA, and .---blank.only in DNA. |
uracil thymine |
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The base .---blank. is a pyrimidine base found only in ribonucleic acids. |
uracil |
|
The sugar component of RNA is ribose, as the name ribonucleic acid implies. In deoxyribonucleic acid (DNA), the sugar is deoxyribose. The deoxy- prefix denotes the absence of a .---blank. which is present in ribose. |
hydroxy group |
|
The sugar component of DNA is called .---blank.. |
deoxyribose |
|
The nucleotides are joined together in nucleic acids by .---blank. that connect the 5' carbon of one nucleotide to the 3' carbon of the next. These linkages are referred to as phosphodiester bonds |
phosphate groups |
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Nucleotides are joined together by .---blank. bonds. |
phosphodiester |
|
The sugar-phosphate chain is referred to as the .---blank. backbone |
nucleic acid |
|
The nucleic acid backbone consists of the .---blank. chain. |
sugar-phosphate |
|
Watson and Crick, from various experimental data, theorized that a secondary structure of DNA consists of two strands entwined around each other in a .---blank. |
double helix |
|
The secondary structure of DNA contains two strands of DNA that form a .---blank. helix. |
double |
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The two intertwined polynucleotide chains of the DNA double helix run in opposite (antiparallel) directions. Thus, each end of the double helix contains the 5' end of one chain and the .---blank. end of the other. |
3' |
|
Two polynucleotide chains running in opposite directions are said to be .---blank. . |
antiparallel |
|
The DNA structure is stabilized by hydrogen bonding between the bases that extend inward from the .---blank. backbone. |
sugar-phosphate |
|
.---blank. interactions between atoms in the base portion of nucleotides provide the stabilizing force to the double helix. |
hydrogen bonding |
|
Complimentary DNA strands are two strands of DNA in a double helix with matching bases forming .---blank. . The most common complimentary base pairs in double-helical DNA are the thymine-adenine pair and the guanine-cytosine base pair. In either case, a purine base hydrogen bonds with a pyrimidine base. In the case of the A-T interaction, 2 hydrogen bonds are involved. For the C-G interaction 3 hydrogen bonds are involved. |
hydrogen bonds |
|
The two most common base pairs in DNA double helixes are the thymine- adenine pair and the guanine-_____________ base pair. |
cytosine |
|
Give two reasons why adenine cannot hydrogen bond with gaunine in a DNA double helix. |
1) Both adenine and guanine are purine bases - a purine must interact with a pyrimidine. 2) Adenine only has 2 places to hydrogen bond; whereas, guanine has 3 places to hydrogen bond. |
|
One strand of a DNA molecule has the base sequence of .---blank. (written in the 5' to 3' direction). |
CCATTG |
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What is the base sequence for the complementary strand in the 5' to 3' direction? |
CAATGG |
|
A human cell normally contains 46 structural units called .---blank. |
chromosomes |
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A human cell contains .---blank. chromosomes. |
46 |
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Each chromosome contains one molecule of DNA coiled tightly about a group of small, basic proteins called .---blank. . |
histones |
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.---blank. are the small basic proteins that form the core around which DNA is coiled in chromosomes. |
histones |
|
Individual sections of DNA molecules make up .---blank. , the fundamental units of heredity. Each gene directs the synthesis of a specific protein or, in some cases, a series of proteins. |
genes |
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.---blank. are sections of DNA that are the fundamental units of heredity. |
genes |
|
A bacterial cell may contain .---blank. genes, whereas a human cell contains approximately 30,000 genes. |
1000 |
|
A human cell contains an estimated .---blank. genes. |
30,000 |
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The process by which an exact copy of DNA is produced is called .---blank. . |
replication |
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DNA molecules are copied by a process called .---blank. . |
replication |
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.---blank. replication is a replication process that produces DNA molecules containing one strand from the parent and a new strand that is complementary to the strand from the parent |
Semiconservative |
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The type of replication process that produces a DNA copy with a new strand and one from the parent is known as .---blank. replication. |
Semiconservative |
|
Step one in the replication process is the unwinding of the double helix catalyzed by the enzyme .---blank. . |
helicase |
|
.---blank. is the enzyme that catalyzes the unwinding of the double helix in the first step of DNA replication. |
helicase |
|
The point at which the unwinding of the double helix takes place is called the .---blank. |
replication fork |
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Helix unwinding is initiated at the .---blank. . |
replication fork |
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Step two of DNA replication involves synthesis of DNA segments. New daughter strands form as nucleotides, complementary to those on the exposed strands, are linked together under the influence of the enzyme .---blank. |
DNA polymerase |
|
The enzyme .---blank. is responsible for the synthesis of DNA. |
DNA polymerase |
|
DNA polymerase synthesizes the daughter chains in the .---blank. to the 3' direction. |
5’ |
|
The direction of growth of the DNA daughter chain is from the .---blank. end. |
5’ |
|
.---blank. fragments are DNA fragments produced during replication as a result of strand growth in a direction away from the replication fork. |
Okazaki |
|
Because growth of one strand proceeds away from the replication fork, .---blank. fragments are formed |
Okazaki |
|
Step 3 of DNA replication involves closing the nicks between the .---blank. fragments on one strand of the newly synthesized DNA. The other daughter strand contains a continuous chain of nucleotides and does not require this process. |
Okazaki |
|
The final step of DNA replication involves closing nicks between .---blank. fragments on one strand. |
Okazaki |
|
An enzyme called .---blank. is responsible for catalyzing the joining of the Okazaki fragments. |
DNA ligase |
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Okazaki fragments are joined by the enzyme .---blank. . |
DNA ligase |
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Through detailed understanding of DNA replication, a revolutionary laboratory technique called the polymerase chain reaction (PCR) was born. .---blank. mimics the natural DNA replication process in a controlled laboratory environment. |
PCR |
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The .---blank. technique is a process through which scientists duplicate natural DNA replication outside living cells. |
PCR |
|
The primary structure of RNA differs from that of DNA in two ways. As we learned in Section 11.1, the sugar unit in RNA is ribose rather than deoxyribose. The other difference is that RNA contains the base .---blank. (U) instead of thymine (T). |
uracil |
|
The base .---blank. is found in RNA in place of thymine. |
uracil |
|
The secondary structure of RNA is also different from that of DNA. RNA molecules are .---blank. -stranded, except in some viruses. |
single |
|
RNA molecules exist primarily as .---blank. strands. |
single |
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Cells contain three types of RNA: messenger RNA (mRNA), ribosomal RNA (rRNA), and transfer RNA (tRNA). Each of these kinds of RNA performs an important function in .---blank. synthesis. |
proteins |
|
RNA molecules are involved in the synthesis of .---blank. . |
proteins |
|
.---blank. (mRNA) functions as a carrier of genetic information from the DNA of the cell nucleus directly to the cytoplasm. |
messenger RNA |
|
Genetic information is carried from the cell nucleus to the cytoplasm via .---blank. . |
messenger RNA |
|
Molecules of mRNA have a short .---blank. , usually less than 1 hour. |
lifetime |
|
In general terms, the turnover rates for mRNA are .---blank. . |
rapid |
|
A .---blank. is a subcellular particle that serves as the site of protein synthesis in all organisms. |
ribosome |
|
.---blank. function as the site of protein synthesis. |
ribosomes |
|
.---blank. RNA (rRNA) constitutes 80-85% of the total RNA of the cell. It is located in the cytoplasm in organelles called ribosomes. |
ribosomal |
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.---blank. RNA makes up the majority of a cell's RNA. |
ribosomal |
|
.---blank. molecules deliver amino acids, the building blocks of proteins, to the site of protein synthesis. |
transfer RNA |
|
Amino acids are delivered to ribosomes via .---blank. . |
transfer RNA |
|
The .---blank. molecules are the smallest of all the nucleic acids, containing 73-93 nucleotides per chain. |
tRNA |
|
The smallest of the nucleic acid molecules are those of .---blank. . |
tRNA |
|
Two regions of tRNA molecules have important functions during protein synthesis. The .---blank. enables the tRNA to bind to mRNA during protein synthesis |
anticodon |
|
The .---blank. portion of tRNA molecule is the binding site for mRNA during protein synthesis. |
anticodon |
|
The second important site of tRNA is the .---blank. end of the molecule, which binds to an amino acid and transports it to the site of protein synthesis. |
3’ |
|
The .---blank. end of the tRNA molecule is the binding site for the amino acid it carries. |
3’ |
|
The central dogma of molecular biology is the well-established process by which genetic information stored in DNA molecules is expressed in the structure of synthesized .---blank. . |
protein |
|
The process by which genetic information is expressed in .---blank. structure constitutes the central dogma of molecular biology. |
protein |
|
Genetic information contained in DNA molecules is transferred to .---blank. molecules, followed by expression of this information in the structure of synthesized proteins. |
RNA |
|
.---blank. provide the link between genetic information stored in DNA and the structure of proteins. |
RNA |
|
Before proteins can be synthesized, the stored information must be carried out of the nucleus. This is accomplished by .---blank. , or transferring the necessary information from the DNA molecule onto a molecule of messenger RNA |
transcription |
|
.---blank. refers to the transfer of genetic information from DNA to mRNAs. |
transcription |
|
The mRNA serves as a template on which amino acids are assembled in the proper sequence necessary to produce the specified protein. This process, called .---blank. , takes place when the code or message carried by mRNA is converted into an amino acid sequence. |
translation |
|
.---blank. refers to the synthesis of a protein according to the code on the corresponding mRNA molecule. |
translation |
|
An enzyme called .---blank. catalyzes the synthesis of RNA. RNA polymerase reads the DNA from the 3' end of the DNA segment to the 5' end; however, it synthesizes RNA from the 5' end to the 3', similar to DNA replication. |
RNA polymerase |
|
The synthesis of RNA is catalyzed by .---blank. . |
RNA polymerase |
|
RNA transcription occurs in the .---blank. to .---blank. direction, while the reading of the DNA occurs in the .---blank. to .---blank. direction. |
5' to 3' 3' to 5' |
|
Genes of eukaryotic cells are segments of DNA that are "interrupted" by segments that do not code for amino acids. These DNA segments that carry no amino acid code are called .---blank. , and the coded DNA segments are called exons. |
introns |
|
Segments of DNA within coding DNA regions that do not code for amino acids are called .---blank. . |
introns |
|
When transcription occurs in the nuclei of eukaryotic cells, both introns and exons are transcribed. This produces what is called .---blank. nuclear RNA or hnRNA |
heterogeneous |
|
The RNA produced in the nuclei of eukaryotic cells containing RNA transcribed from both introns and exons is called .---blank. nuclear RNA. |
heterogeneous |
|
The long hnRNA molecule undergoes a series of enzyme-catalyzed reactions that cut and splice the hnRNA to produce .---blank. . Once the introns have been removed and mRNA has been made from the hnRNA, it can leave the nucleus to provide directions for protein synthesis in the cytoplasm. |
mRNA |
|
In order to form .---blank. from hnRNA, the noncoding regions must first be cut and then the coding regions joined together. |
mRNA |
|
When a protein is synthesized, it will only contain information from the (introns/exons) of the DNA sequence. |
exons |
|
Nature uses three-letter code words to store and express genetic information. Each sequence of three nucleotide bases that represents code words on mRNA molecules is called a .---blank. |
codons |
|
The three letter codes that store and express genetic information are called .---blank. . |
codons |
|
A three base code has 43 or .---blank. possible combinations. |
64 |
|
There are .---blank. possible codons. |
64 |
|
One important characteristic of the genetic code is that it applies to every organism (see Table 11.3). The code is almost .---blank. from species to species. |
universal |
|
The genetic code is almost .---blank. , differing only rarely from species to species. |
universal |
|
A second feature of the genetic code is that most of the amino acids are represented by more than one codon, a characteristic known as degeneracy. .---blank. helps remove the effects of any mutations caused by changes in base pairs by increasing the chances that the correct amino acid will still be coded for. |
Degeneracy |
|
a) The genetic code is said to be .---blank. when an amino acid is represented by more than one codon. |
degenerate |
|
The codons that signal for phenylalanine are UUC and UUU. If the codon were UUU and the third nucleotide was changed (mutated), what are the chances that phenyl-alanine would still be coded for? |
UUU could be mutated to UUC, UUG, and UUA. UUC still codes for phenylalanine, so there would be a 1/3 or 33% chance that phenylalanine would still be coded for. |
|
Only 61 of the possible 64 base triplets represent amino acids. The remaining three (UAA, UAG, UGA) are signals for .---blank. . |
chain termination |
|
Codons that do not code for amino acids are signals for .---blank. . |
chain termination |
|
There is only one initiation (start) codon, and it is AUG, the codon for the amino acid .---blank. . |
methionine |
|
AUG, the chain initiation signal, codes for the amino acid .---blank. . |
methionine |
|
There are three major stages in protein synthesis: initiation of the polypeptide chain, .---blank. of the chain, and termination of the completed polypeptide chain |
elongation |
|
The three steps of protein synthesis are initiation, .---blank. and termination. |
elongation |
|
The initiation process begins when mRNA is aligned on the surface of a small ribosomal subunit in such a way that the initiating codon, AUG, occupies a specific site on the ribosome called the .---blank. site (peptidyl site). |
P |
|
The initiating codon of the mRNA must occupy the .---blank. site of the ribosome for the initiation process to begin. |
P |
|
A tRNA molecule with its attached f-Met binds to the codon through hydrogen bonds. The resulting complex binds to the large ribosomal subunit to form a unit called an .---blank. .--- |
initiation complex |
|
Upon binding of the large ribosomal subunit to the mRNA, followed by binding of the small ribosomal subunit and the f-Met tRNA molecule, the .---blank. complex is complete, enabling the next step of protein synthesis to commence. |
initiation |
|
A second site, called the .---blank. site (aminoacyl site), is located on the mRNA-ribosome complex next to the P-site. The A site is occupied by an incoming tRNA carrying the next amino acid. Each codon that codes for an amino acid on the mRNA consists of 3 nucleotide bases. |
A |
|
a) The binding site for incoming tRNA molecules adjacent to the P site is called the .---blank. . |
A site |
|
b) A polypeptide is 6 amino acids long. How many nucleotides on an mRNA strand are necessary to code for this polypeptide? |
6 x 3 = 18 nucleotides |
|
After a tRNA molecule binds to the A-site, the whole ribosome moves one codon along the mRNA toward the 3' end. This movement of the ribosome along the mRNA is called .---blank. , during which the A site becomes available to the next tRNA with the proper anticodon |
translocation |
|
.---blank. is the process by which the ribosome moves along the mRNA molecule. |
translocation |
|
The chain elongation process and polypeptide synthesis continue until the ribosome complex reaches a .---blank. (UAA, UAG, UGA) on the mRNA. |
stop codon |
|
The presence of a .---blank. codon results in termination of polypeptide synthesis. |
stop |
|
Several .---blank. can move along a single strand of mRNA one after another. Complexes of several ribosomes and mRNA are called polyribosomes or polysomes |
ribosomes |
|
Polyribosomes contain several .---blank. on a single mRNA strand. |
ribosomes |
|
Any change resulting in an incorrect sequence of bases on DNA is called a .---blank. . |
Mutation |
|
A .---blank. is a change resulting in an incorrect sequence of DNA bases. |
mutation |
|
Some mutations occur naturally during DNA replication; others can be induced by environmental factors such as ionizing radiation (X rays, ultraviolet light, gamma rays, etc.). A large number of chemicals (e.g. nitrous acid and dimethyl sulfate) can also induce mutations by reacting with DNA. Such chemicals are called .---blank. . |
mutagens |
|
DNA mutations can occur naturally during DNA replication, or by environmental factors such as .---blank. radiation, or as the result of exposure to chemicals called .---blank. . |
ionizing, mutagens |
|
Remarkable technology is available that allows segments of DNA from one organism to be introduced into the genetic material of another organism. The resulting new DNA (containing the foreign segment) is referred to as .---blank. . |
recombinant DNA |
|
DNA of an organism that contains genetic material from another organism is called .---blank. DNA. |
recombinant |
|
The discovery of restriction enzymes in the 1960s and 1970s made genetic engineering possible. .---blank. enzymes are protective enzymes found in a wide variety of bacteria catalyzing the cleaving of foreign DNA at specific sequences. |
restricition |
|
Enzymes that catalyze the cleavage of foreign DNA in specific sequences are called .---blank. enzymes. |
restricition |
|
Another set of enzymes important in genetic engineering, called .---blank. , has been known since 1967. These enzymes normally function to connect DNA fragments during replication, and they are used in genetic engineering to put together pieces of DNA produced by restriction enzymes. |
DNA ligase |
|
In genetic engineering, pieces that are cleaved by restriction enzymes are connected through the use of .---blank. . |
DNA ligase |
|
The introduction of a new DNA segment (gene) into a bacterial cell requires the assistance of a DNA carrier called a .---blank. . |
vectors |
|
.---blank. are DNA carriers used in genetic engineering to introduce foreign DNA into the desired cell. |
vectors |
|
Vectors are often circular units of double-stranded DNA called .---blank. , which are isolated from the cytoplasm of bacterial cells. |
plasmids |
|
Circular units of DNA often used as vectors are called .---blank. . |
plasmids |