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This set of flashcards encompasses key vocabulary and concepts related to gene expression, genetic mutations, genetic disorders, and biotechnological techniques.
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MicroRNAs (miRNAs)
Small non-coding RNA molecules that regulate gene expression by binding to mRNA.
Polycistronic mRNA
mRNA that codes for more than one protein, typically found in prokaryotes.
Monocistronic mRNA
mRNA that codes for a single protein, typically found in eukaryotes.
Operon
A cluster of functionally related genes under the control of a single promoter, found in prokaryotes.
Trp Operon
A repressible operon that is active in the absence of tryptophan.
Lac Operon
An inducible operon that is expressed in the presence of lactose.
Enhancers
Short regions of DNA that bind proteins to promote the expression of genes.
Promoters
Regions of DNA that initiate transcription by binding RNA polymerase.
TATA Box
A DNA sequence that binds transcription factors to regulate gene expression.
Transcriptional Start Site
The location within the promoter where transcription begins.
Open Reading Frame (ORF)
The part of a gene that codes for a protein, starting with an ATG and ending with a stop codon.
Genetic Mosaicism
Presence of two or more different populations of cells with different genotypes in one organism.
Chimerism
Fusion of more than one fertilized zygote early in development, resulting in an organism with cells from different zygotes.
Mutagenesis
The process of making mutations, often induced by radiation or chemicals.
Forward Genetics
Approach where mutations are randomly made and screened for desired phenotypes.
Reverse Genetics
Method to identify the phenotype resulting from a specific gene mutation.
Erameshift mutation
Mutation resulting from addition or deletion of nucleotides, shifting the reading frame of the gene.
Nonsense mutation
A mutation that creates a premature stop codon in the protein sequence.
Trinucleotide Repeats
Repeats of a short sequence of three nucleotides in a gene associated with genetic disorders.
Defective Genes
Genes that do not produce the correct protein, potentially resulting in genetic disorders.
Nondisjunction
Failure of chromatids to separate properly during meiosis, leading to gametes with abnormal chromosome number.
X-linked Recessive Disorders
Genetic disorders that occur when a defective gene is located on the X chromosome.
Sanger Sequencing
A method for determining the nucleotide sequence of DNA using labeled chained-terminating nucleotides.
CRISPR-Cas9
A genome editing technology that uses a guide RNA and Cas9 enzyme to modify DNA sequences.
Gene therapy
An experimental technique that uses genes to treat or prevent diseases.
Bioethics
Field of study that addresses the ethical implications of biological research and applications.
Epigenetics
Study of heritable changes in gene expression that do not involve changes to the underlying DNA sequence.