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BIO 309 Exam | Human Anatomy & Physiology Questions, Practice Test & Comprehensive Review

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Prepare for the BIO 309 Exam with this comprehensive study resource designed for students reviewing Human Anatomy and Physiology concepts. The material supports preparation across essential anatomy and physiology topics, including body organization, tissues, skeletal and muscular systems, nervous system, cardiovascular system, respiratory system, digestive system, urinary system, reproductive system, endocrine function, lymphatic structures, and physiological processes. Ideal for students searching for BIO 309 exam questions, Human Anatomy study guides, Anatomy & Physiology practice tests, BIO 309 exam review, and biology exam preparation. Because BIO 309 is used for different biology courses by different institutions, the exact course should be verified against the school listed on the original document before publishing the Stuvia listing. Current search results connect BIO 309 with Human Anatomy and Anatomy & Physiology coursework.

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Bio 309 Exam
phenotype the physical, observable expression of a characteristic or trait; "what you see"




wildtype the phenotype we expect to see in wild individuals; notated by x+ where x is the
allele for the gene and defined by having an allele frequency of greater than 1%



mendel's law of independent assortment describes how different alleles of different genes behave individually




linked genes genes that are located near each other on a chromosome and tent to travel
together during meiosis



gene cloning the process of using living cells to make exact replicas of a fragment of foreign
DNA



polymerase chain reaction (PCR) an in vitro method of detection and isolation of genomic fragments using cyclic
repetitions of DNA synthesis reactions; involves a thermostable DNA polymerase
that catalyzes multiple rounds of DNA synthesis, beginning with two primers that
flank a region of interest within a target DNA template


forward primer the PCR primer with the same sequence as the top strand, and binds to the
bottom strand



reverse primer the PCR primer with the same sequence as the bottom strand, that binds to the
top strand



genetically modified organisms (GMO) an organism whose genome has been engineered to have a desirable phenotype




covalent bond a strong type of chemical bond in which two atoms share one or more pairs of
electrons



endonucleases an enzyme that cleaves the phosphodiester bond within a polynucleotide tail (ie.
DNA)



exonucleases an enzyme that removes successive nucleotides from the end of a
polynuncleotide (ie. DNA)



restriction endonucleases endonucleases that cut DNA at specific positions




denaturation the reversible process of unfolding a protein or DNA




renature the process of refolding unfolded protein or DNA strands




hydrophobic interactions interactions between non-polar chemical groups or molecules, and polar water

, Bio 309 Exam
supercoiling the effect on DNA where the double helix is coiled on itself




open circular form the relaxed, non-supercoiled form of a plasmid that has broken a strand of DNA




covalently closed circular form the natural, supercoiled for of plasmid




open reading frame (ORF) a continuous stretch of codons that begins with a start codon and ends at a stop
codon (ie. the part of a reading frame that has the ability to be translated)



consensus sequence a sequence of DNA in a promoter that is similar in all genes eg. TATA consensus
sequence (TATA box)



trans-acting element a factor that regulates gene expression but is not located on that gene eg.
repressor proteins



cis-acting element factors coded for within DNA that regulate gene expression for that gene eg.
binding sites for trans-acting elements



enhancer a regulatory site that increases transcription; can be located far away (can be
10,000 base pairs away) from the core promoter, or can be quite close; cis acting



exon coding sequence for the promoter product; sequences found in both a gene's
DNA and in the mature mRNA



intron non-coding sequences found in a gene's DNA but not in the mature mRNA;
removed from the primary transcript during splicing



shine-dalgarno sequence a sequence of the ribosome binding site in bacteria, generally located about 8
bases upstream of the start codon AUG; helps recruit the ribosome to the mRNA
to initiate translation by aligning the ribosome with the start codon


operon a unit of DNA composed of specific genes, plus a promoter and an operator,
which act in unison to regulate the response of the structural genes to
environmental changes


epigenetic phenomena changes in gene expression not related to sequence changes




RNA interference the action of miRNAs to alter mRNA stability and translational efficiency to
reduce protein production



alternative splicing the regulated process during gene expression that results in a single gene
coding for multiple possible proteins through different splicing patterns (ie.
removal of different segments as introns)


upstream before the transcription start site

, Bio 309 Exam
downstream after the transcription start site




fusion protein a protein created through the joining of two or more genes that originally coded
for separate proteins



translational fusion the joining of genetic information affecting the translation of a protein product, to
result in a fusion protein



transcriptional fusion fusion at the transcriptional level to produce a fusion protein product; aka.
promoter::reporter fusions; replacing the coding region of a gene with the coding
sequence for reporter gene to monitor the activity of a promoter


reporter genes genes that are easily detectable and are used to: monitor protein location,
movement, interactions (ie. translational fusions), or monitor promoter activity
(eg. transcriptional fusions) eg. luciferase, green fluorescent protein, Lac Z


induction the process by which a tissue or cell directs neighbouring tissues or cells to
develop in a specific way



genetic approach an in vivo approach to studying molecular biology in which we study organisms
with mutations in specific genes to learn about the function of corresponding
gene products (ie. requires functional organisms)


forward genetics a type of genetic approach in which we find a mutant first, then identify what
caused the phenotype, genetically; ie. analyze phenotype --> analyse gene eg.
Mendel and his peas


reverse genetucs a type of genetic approach in which we start with a gene of interest, then create
an organism that expressed that gene abnormally (ie. mutant) due to the
introduction of additional sequences (transgenes); includes gene silencing; ie.
analyze the gene --> analyze phenotype


biochemical approach an in vitro approach to studying molecular biology in which we study proteins or
metabolites (ie. activity, structures, etc.)(ie. does not require a functional
organism)


bioinformatic approach an in silico approach to studying molecular biology in which we create databases
of large data sets and develop query algorithms to mine data to make
experimental predictions and biological models (ie. requires computers)


screen the act of analyzing every member of a population to identify which are abnormal
for the trait in question



select isolation of the mutant in question, after screening




transgene a gene that has been introduced into the genome artificially




biochemistry the study of proteins and enzyme activities




homogenate a component of a biochemical approach that maintains the functionality of the
protein of interest using a pH buffer, salts, cofactors, and protease inhibitorsl;
aka. extract

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