Bacterial and Eukaryotic Genetics Lecture Review

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Comprehensive vocabulary flashcards covering linked genes, bacterial genetic transfer, transcription, translation, mutations, DNA repair, and genetic testing based on the provided lecture notes.

Last updated 8:39 PM on 7/16/26
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70 Terms

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Linked genes

Genes located close together on the same chromosome that tend to be inherited together.

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Unlinked genes

Genes located far apart on a chromosome or on different chromosomes that assort independently.

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Parental/noncrossover genes

Allele combinations that match the original parental chromosome because no crossover occurred between them.

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Recombinant/crossover genes

Allele combinations that differ from the parental arrangement because a crossover occurred between the loci.

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Single crossover

One crossover event occurring between two linked genes during meiosis.

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Double crossover

Two crossover events occurring between two linked genes, which can restore the parental allele arrangement.

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Recombination Frequency (RF)

The probability of crossing over occurring between two genes, calculated as: RF=(number of recombinant offspringtotal offspring)×100%RF = (\frac{\text{number of recombinant offspring}}{\text{total offspring}}) \times 100\%

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Map Unit (cM)

A unit of distance on a genetic map where 1% recombination frequency=1 map unit1\%\ \text{recombination frequency} = 1\ \text{map unit} (also called 1 centiMorgan).

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Physical map

A map showing the actual physical distance between genes on a chromosome, usually measured in base pairs (bpbp) based on DNA sequence data.

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Genetic (linkage) map

A map showing the relative distance between genes based on recombination frequency (map units/cMmap\ units/cM).

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Conjugation

Direct transfer of DNA between bacterial cells through a physical connection called a pilus.

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Transformation

The uptake of free DNA from the environment by a bacterial cell.

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Transduction

The transfer of bacterial DNA from one cell to another via a bacteriophage.

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Cotransformation

The simultaneous uptake and incorporation of two or more genes during transformation, indicating they are close together.

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Cotransduction

The simultaneous transfer of two or more genes by a single phage particle, indicating they are close together.

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Vertical gene transfer

The transmission of genetic material from parent to offspring.

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Horizontal gene transfer

The transmission of genetic material between organisms that are not parent and offspring.

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Bacteriophage

A virus that infects bacteria.

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F+ cell

A bacterial cell that contains the F (fertility) plasmid and can act as a DNA donor in conjugation.

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F- cell

A bacterial cell that lacks the F plasmid and acts as a DNA recipient in conjugation.

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Hfr cell

\"High frequency of recombination\" cell, in which the F plasmid has integrated into the bacterial chromosome, allowing efficient transfer of chromosomal genes.

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F’ plasmid

An F plasmid that has excised from the chromosome carrying adjacent bacterial genes with it.

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Partial diploid

A bacterial cell that carries two copies of some genes, one on the chromosome and one on a plasmid (such as an F').

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Prototroph

A \"wild type\" bacterium for a specific gene that can synthesize everything it needs and grows on minimal media.

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Auxotroph

A bacterium that has a mutation in a gene needed to make a specific nutrient and cannot grow on minimal media without that nutrient added (e.g., leuleu^-).

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Lytic cycle

A fast, destructive phage life cycle where the phage takes over the host, assembles new particles, and lyses (bursts) the cell.

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Lysogenic cycle

A phage cycle where the DNA integrates into the host chromosome as a prophage and is copied silently along with the host DNA for generations.

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Template strand

The DNA strand that is read by RNA polymerase and used as the basis for RNA synthesis; also known as the non-coding strand.

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Non-template strand

The DNA strand not used as the template, which matches the RNA transcript sequence (with T instead of U); also known as the coding strand.

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RNA polymerase

The enzyme that synthesizes RNA from a DNA template.

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Holoenzyme

The complete bacterial RNA polymerase complex, consisting of the core enzyme and a sigma factor.

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Transcription factors

Proteins that help regulate the binding of RNA polymerase and the initiation of transcription.

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Promoter

A DNA sequence located near the start of a gene that directs RNA polymerase where to begin transcription.

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Upstream

The direction on DNA opposite to the direction of transcription, toward the 55' end of the coding strand.

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Downstream

The direction on DNA in the direction of transcription, toward the 33' end of the coding strand.

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TATA box

A eukaryotic promoter consensus sequence (TATAAATATAAA) that helps position RNA polymerase II for transcription initiation.

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-10 consensus sequence

A bacterial promoter element located about 10 bp10\ bp upstream of the transcription start site (TATAATTATAAT).

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-35 consensus sequence

A bacterial promoter element located about 35 bp35\ bp upstream of the transcription start site (TTGACATTGACA).

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Introns

Noncoding sequences within a gene that are removed from the pre-mRNA during splicing.

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Exons

Coding sequences within a gene that are retained in the mature mRNA after splicing.

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Splicing

The process of removing introns and joining exons together to form mature mRNA.

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RNA processing

The modifications (capping, splicing, polyadenylation) that convert pre-mRNA into mature mRNA in eukaryotes.

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5’ cap

A modified guanine nucleotide added to the 55' end of pre-mRNA to protect it from degradation and help the ribosome bind.

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Poly-A tail

A long string of adenine nucleotides added to the 33' end of mRNA that protects it from degradation and aids in nuclear export.

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snRNAs

Small nuclear RNAs that form spliceosome components to catalyze splicing.

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snRNP

A small nuclear ribonucleoprotein complex (snRNA + proteins) that is a component of the spliceosome.

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Codon

A three-nucleotide sequence in mRNA that specifies a particular amino acid or a stop signal.

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Anticodon

A three-nucleotide sequence on tRNA that base-pairs with a complementary codon on mRNA.

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Start codon

The codon (AUGAUG) that signals the beginning of translation and codes for methionine.

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Stop codon

A codon that signals the end of translation (UAAUAA, UAGUAG, or UGAUGA).

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Reading frame

The way an mRNA sequence is divided into consecutive, non-overlapping codons during translation.

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Aminoacyl-tRNA synthetase

The enzyme that attaches a specific amino acid to its corresponding tRNA.

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Shine-Dalgarno sequence

A bacterial ribosome-binding sequence (AGGAGGAGGAGG) located upstream of the start codon.

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Kozak sequence

A eukaryotic consensus sequence (GCCRCCAUGGGCCRCCAUGG, where R=purineR = purine) that promotes efficient translation initiation.

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Spontaneous mutation

A mutation that arises naturally, without exposure to an external mutagenic agent.

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Induced mutation

A mutation caused by exposure to an external mutagen such as chemicals or radiation.

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Mutagen

An agent that increases the rate of mutation.

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Base-substitution mutation

A mutation in which one nucleotide base is replaced by another.

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Frameshift mutation

A mutation caused by insertion or deletion of nucleotides that shifts the reading frame of the gene.

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Thymine dimer

A DNA lesion where two adjacent thymine bases become covalently linked, often due to UV light exposure.

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Depurination

A spontaneous mutation where a purine base (AA or GG) is chemically removed from the sugar-phosphate backbone.

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Deamination

The removal of an amino group from a base, such as converting cytosine into uracil.

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Intercalating agents

Flat molecules that wedge between base pairs, distorting the DNA helix and causing frameshift mutations.

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Transposable elements

DNA sequences (\"jumping genes\") that can move to different locations in the genome, potentially disrupting gene function.

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Mismatch repair

A post-replication repair mechanism where proteins scan DNA for mismatched bases and resynthesize the incorrect section.

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Photoreactive repair

A repair mechanism using photolyase and light energy to break apart thymine dimers.

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Base excision repair

A mechanism where an enzyme removes a single damaged base and DNA polymerase fills in the correct one.

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Nucleotide excision repair

A mechanism that removes a bulky DNA distortion (like a thymine dimer) by cutting out a section of nucleotides and resynthesizing it.

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Nonhomologous end joining

An error-prone repair pathway that fixes double-strand breaks by directly gluing the two broken ends back together without a template.

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BRCA1 and BRCA2

Tumor suppressor genes that normally produce proteins involved in repairing double-strand DNA breaks via homologous recombination repair.