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47 Cards in this Set
- Front
- Back
5′ cap |
A modified form of guanine nucleotide added onto the 5′ end of a pre-mRNA molecule. |
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A site |
One of a ribosome’s three binding sites for tRNA during translation. The A site holds the tRNA carrying the next amino acid to be added to the polypeptide chain. (A stands for aminoacyl tRNA.) |
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alternative RNA splicing |
A type of eukaryotic gene regulation at the RNA-processing level in which different mRNA molecules are produced from the same primary transcript, depending on which RNA segments are treated as exons and which as introns. |
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aminoacyl-tRNA synthetase |
An enzyme that joins each amino acid to the appropriate tRNA. |
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anticodon (an′-tī-kō′-don) |
A nucleotide triplet at one end of a tRNA molecule that base-pairs with a particular complementary codon on an mRNA molecule. |
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codon (kō′-don) |
A three-nucleotide sequence of DNA or mRNA that specifies a particular amino acid or termination signal; the basic unit of the genetic code. |
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exon |
A sequence within a primary transcript that remains in the RNA after RNA processing; also refers to the region of DNA from which this sequence was transcribed. |
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frameshift mutation |
A mutation occurring when nucleotides are inserted in or deleted from a gene and the number inserted or deleted is not a multiple of three, resulting in the improper grouping of the subsequent nucleotides into codons. |
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gene expression |
The process by which information encoded in DNA directs the synthesis of proteins or, in some cases, RNAs that are not translated into proteins and instead function as RNAs. |
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insertion |
A mutation involving the addition of one or more nucleotide pairs to a gene. |
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intron (in′-tron) |
A noncoding, intervening sequence within a primary transcript that is removed from the transcript during RNA processing; also refers to the region of DNA from which this sequence was transcribed. |
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messenger RNA (mRNA) |
A type of RNA, synthesized using a DNA template, that attaches to ribosomes in the cytoplasm and specifies the primary structure of a protein. (In eukaryotes, the primary RNA transcript must undergo RNA processing to become mRNA.) |
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missense mutation |
A nucleotide-pair substitution that results in a codon that codes for a different amino acid. |
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mutagen (myū′-tuh-jen) |
A chemical or physical agent that interacts with DNA and can cause a mutation. |
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mutation (myū-tā′-shun) |
A change in the nucleotide sequence of an organism’s DNA or in the DNA or RNA of a virus. |
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nonsense mutation |
A mutation that changes an amino acid codon to one of the three stop codons, resulting in a shorter and usually nonfunctional protein. |
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nucleotide-pair substitution (nū′-klē-ō-tīd′) |
A type of point mutation in which one nucleotide in a DNA strand and its partner in the complementary strand are replaced by another pair of nucleotides. |
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P site |
One of a ribosome’s three binding sites for tRNA during translation. The P site holds the tRNA carrying the growing polypeptide chain. (P stands for peptidyl tRNA.) |
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point mutation |
A change in a single nucleotide pair of a gene. |
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poly-A tail |
A sequence of 50–250 adenine nucleotides added onto the 3′ end of a pre-mRNA molecule. |
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polyribosome (polysome) (pol′-ē-rī′-buh-sōm′) |
A group of several ribosomes attached to, and translating, the same messenger RNA molecule. |
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primary transcript |
An initial RNA transcript from any gene; also called pre-mRNA when transcribed from a protein-coding gene. |
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primase |
An enzyme that joins RNA nucleotides to make a primer during DNA replication, using the parental DNA strand as a template. |
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promoter |
A specific nucleotide sequence in the DNA of a gene that binds RNA polymerase, positioning it to start transcribing RNA at the appropriate place. |
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reading frame |
On an mRNA, the triplet grouping of ribonucleotides used by the translation machinery during polypeptide synthesis. |
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ribosomal RNA (rRNA) (rī′-buh-sō′-mul) |
RNA molecules that, together with proteins, make up ribosomes; the most abundant type of RNA. |
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ribosome (rī′-buh-sōm) |
A complex of rRNA and protein molecules that functions as a site of protein synthesis in the cytoplasm; consists of a large and a small subunit. In eukaryotic cells, each subunit is assembled in the nucleolus. See alsonucleolus. |
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ribozyme (rī′-buh-zīm) |
An RNA molecule that functions as an enzyme, such as an intron that catalyzes its own removal during RNA splicing. |
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RNA polymerase |
An enzyme that links ribonucleotides into a growing RNA chain during transcription, based on complementary binding to nucleotides on a DNA template strand. |
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RNA processing |
Modification of RNA primary transcripts, including splicing out of introns, joining together of exons, and alteration of the 5′ and 3′ ends. |
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RNA splicing |
After synthesis of a eukaryotic primary RNA transcript, the removal of portions of the transcript (introns) that will not be included in the mRNA and the joining together of the remaining portions (exons). |
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signal peptide |
A sequence of about 20 amino acids at or near the leading (amino) end of a polypeptide that targets it to the endoplasmic reticulum or other organelles in a eukaryotic cell. |
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signal-recognition particle (SRP) |
A protein-RNA complex that recognizes a signal peptide as it emerges from a ribosome and helps direct the ribosome to the endoplasmic reticulum (ER) by binding to a receptor protein on the ER. |
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silent mutation |
A nucleotide-pair substitution that has no observable effect on the phenotype; for example, within a gene, a mutation that results in a codon that codes for the same amino acid. |
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spliceosome (splī′-sō-sōm) |
A large complex made up of proteins and RNA molecules that splices RNA by interacting with the ends of an RNA intron, releasing the intron and joining the two adjacent exons. |
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start point |
In transcription, the nucleotide position on the promoter where RNA polymerase begins synthesis of RNA. |
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TATA box |
A DNA sequence in eukaryotic promoters crucial in forming the transcription initiation complex. |
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template strand |
The DNA strand that provides the pattern, or template, for ordering, by complementary base pairing, the sequence of nucleotides in an RNA transcript. |
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terminator |
In bacteria, a sequence of nucleotides in DNA that marks the end of a gene and signals RNA polymerase to release the newly made RNA molecule and detach from the DNA. |
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transcription |
The synthesis of RNA using a DNA template. |
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transcription factor |
A regulatory protein that binds to DNA and affects transcription of specific genes. |
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transcription initiation complex
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The completed assembly of transcription factors and RNA polymerase bound to a promoter. |
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transcription unit |
A region of DNA that is transcribed into an RNA molecule. |
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transfer RNA (tRNA) |
An RNA molecule that functions as a translator between nucleic acid and protein languages by carrying specific amino acids to the ribosome, where they recognize the appropriate codons in the mRNA. |
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translation |
The synthesis of a polypeptide using the genetic information encoded in an mRNA molecule. There is a change of “language” from nucleotides to amino acids. |
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triplet code |
A genetic information system in which sets of three-nucleotide-long words specify the amino acids for polypeptide chains. |
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wobble |
Flexibility in the base-pairing rules in which the nucleotide at the 5′ end of a tRNA anticodon can form hydrogen bonds with more than one kind of base in the third position (3′ end) of a codon. |