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GNRS 515 Advanced Pathophysiology Exam Questions and Answers 100% Pass

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2COPYRIGHT © 2025 BY SOPHIA BENNETT, ALL RIGHTS RESERVED Translation - RNA to protein (uracil replaces thymine) mRNA - synthesized from DNA by RNA polymerase. Uses tRNA (by binding to ribosome) to sequence amino acids Transcription factors - also binds to DNA & regulates the transcription timing. Can turn on/off gene expression Epigenetics - is the study of heritable changes in gene expression (phenotype) caused by mechanisms other than changes in DNA (nucleotide) sequences; e.g. when a somatic cell divides (mitotic inheritance), when gametes are produced (germline inheritance), or both epigenetic modification - Epigenetic modifications can cause individuals with the same DNA sequences (such as identical twins) to have different disease profiles functional mRNA - carries genetic information from DNA to Ribosome present in cytosol, where it is used as a template for protein synthesis Introns (removed); exons - which are the removed and remaining sequences after remaining DNA sequences are spliced exome - remaining exon sequence RNA splicing - taking mRNA rough draft and making it into an mRNA final sequence tRNA - directs protein synthesis with mRNA and has a site for attachment of an AA (anticodon) microRNA (miRNA) - small RNA sequences that bind to specific mRNA sequences & down-regulate their expression 3COPYRIGHT © 2025 BY SOPHIA BENNETT, ALL RIGHTS RESERVED small interfering RNA (siRNA) - used in cancer and gene therapy. not translated in DNA sequence long noncoding RNA (lncRNA) - involved in gene regulation; the genome contains is least 10k long gamete or somatic cell, which one is sperm? - gamete: human sex cell gamete composition - has 23 chromosomes (haploid cell) autosome - first 22 of the 23 pairs of chromosomes (not the sex chromosome) karyotype - ordered display of the pairs of chromosomes from a cell; according to size How are homologous chromosomes paired together in a karyotype? - by length and centromere location Describe the two arms of the chromosome - all of them have it, and the center is at the centromere Chances of major chromosome abnormality - 1 in 150 live births Haploid vs. Diploid cell - 23 vs 46 polyploid - more than the diploid number of chromosomes (low survivability, 10% miscarriage) triploidy - zygote with more than the four copies of each chromosome (92); (low survivability - 10% miscarriage) Aneuploidy - Abnormal number of chromosom

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GNRS 515 Advanced Pathophysiology
Exam Questions and Answers 100%
Pass


DNA replication - ✔✔untwisted and zipped by hydrogen bonds being broken between
two pairs

DNA polymerase - ✔✔pairs new bases, aka complementary base pairing (ATCG)

Chromosome aberrations occur where? - ✔✔occurs among number or structure

Explain base pair substitution - ✔✔mutation where ATCG base pairing is mixed

Missense mutation - ✔✔A base-pair substitution that results in a codon that codes for a
different amino acid. The "sense" of the codon is altered

Nonsense mutation - ✔✔substitutions into a stop codon, but it is in the wrong place!
(quite dangerous)

Silent mutation - ✔✔nucleotide change does not affect amino acid

Frameshift mutation - ✔✔insertion or deletion of one or more base pairs. Changes the
entire reading frame of DNA sequence (also dangerous)

Codons - ✔✔consist of a group of three amino acids that start or stop DNA processing

Transcription - ✔✔DNA to RNA (uracil replaces thymine)



COPYRIGHT © 2025 BY SOPHIA BENNETT, ALL RIGHTS RESERVED 1

, Translation - ✔✔RNA to protein (uracil replaces thymine)

mRNA - ✔✔synthesized from DNA by RNA polymerase. Uses tRNA (by binding to
ribosome) to sequence amino acids

Transcription factors - ✔✔also binds to DNA & regulates the transcription timing. Can
turn on/off gene expression

Epigenetics - ✔✔is the study of heritable changes in gene expression (phenotype)
caused by mechanisms other than changes in DNA (nucleotide) sequences; e.g. when a
somatic cell divides (mitotic inheritance), when gametes are produced (germline
inheritance), or both

epigenetic modification - ✔✔Epigenetic modifications can cause individuals with the
same DNA sequences (such as identical twins) to have different disease profiles

functional mRNA - ✔✔carries genetic information from DNA to Ribosome present in
cytosol, where it is used as a template for protein synthesis

Introns (removed); exons - ✔✔which are the removed and remaining sequences after
remaining DNA sequences are spliced

exome - ✔✔remaining exon sequence

RNA splicing - ✔✔taking mRNA rough draft and making it into an mRNA final
sequence

tRNA - ✔✔directs protein synthesis with mRNA and has a site for attachment of an AA
(anticodon)

microRNA (miRNA) - ✔✔small RNA sequences that bind to specific mRNA sequences
& down-regulate their expression




COPYRIGHT © 2025 BY SOPHIA BENNETT, ALL RIGHTS RESERVED 2

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