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MCDB 101B Final (Everything after midterm 2) 2024 Questions With All Correct Solutions!! $12.99   Add to cart

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MCDB 101B Final (Everything after midterm 2) 2024 Questions With All Correct Solutions!!

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MCDB 101B Final (Everything after midterm 2) 2024 Questions With All Correct Solutions!!

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  • October 17, 2024
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68 Multiple choice questions

Term 1 of 68
Non-stop decay

Enzyme that cuts DNA at a specific sequence of nucleotides

Repression of mRNAs lacking stop codons due to mutation or mis-splicing

sequences of amino acids that fold into functional units

label probe, incubate with DBP, gel electrophoresis, detection

Definition 2 of 68
Drosha crops out pre-miRNA stem-loop
Transported into the cytoplasm
Dicer reduces to miRNA
RISC picks up duplex miRNA
Remaining strand serves as the guide in miRISC (contains argonaute protein)




miRNA mechanism


5' cap addition

Direct repression


exon shuffling

,Term 3 of 68
SNPs

Silences genes:
paternally imprinted= paternal allele is silenced
maternally imprinted= maternal allele is silenced


single nucleotide polymorphism (change): one nucleotide at a loci may be mutated, 1 per 1
kb, most common cause of variation


restriction fragment length polymorphisms
Differences among people in their DNA sequences at sites recognized by restriction
enzymes


Small RNAs generated by processing long transcripts. The piRNAs recruit Piwi protein
complexes to transposable element sites in genomic DNA and prevent TE mobilization.

Term 4 of 68
Direct repression

- Prevent binding of basal factors (RNA Pol 2) to promoter, usually with help of co-
repressor.
- Histone modifying enzymes that close the chromatin at promoter

- Activates promoters over long distances, Intervening DNA bends so the enhancer and
promoter can interact
- Detected through deletion analysis
- Flexible orientation/position


Technique for footprinting ribosomes on mRNAs. High throughput sequencing of mRNA
fragments protected by ribosomes can provide information about translation regulation

- Guanine nucleotide added by capping enzyme in reverse orientation to the 5' end of
eukaryotic RNA primary transcript
- Methyl transferases then add methyl groups to form the cap

, Term 5 of 68
Activation domain

Approximately 1000 bp at both ends of a single BAC clone is sequenced. Knowing the two
sequence reads are connected on a single BAC insert allows genome assembly despite the
presence of repeated elements.

Intrinsically disordered domain. Can bind to basal factors or co-activators (can open
chromatin of promoter by degrading nucleosomes)

- Identifies transcriptional start site (+1 position), critical position and orientation
- Contains TATA box approx. 30 nt upstream of start site

production of DNA clones from mRNA sequences using reverse transcription
cDNA library will have genes present for a specific organ

Definition 6 of 68
Allows DNA-binding proteins to interact with other proteins through the leucine zipper
Homodimer: same subunits
Heterodimer: nonidentical subunits

Alternative splicing


Positional cloning

Dimerization domain

Exon junction complex

Definition 7 of 68
manipulation of the genome in order to cure a disease
Focuses on altering the genomes of somatic cells in patients

Basal factors

Gene therapy


cDNA cloning

Non-stop decay

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