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Biol 1406 Exam 4
Meiosis, mitosis, DNA replicaion and Gene expression
| Term | Definition |
|---|---|
| Genome | The complete set of genes in a living organism |
| Chromosomes | Condensed chromatin; called sister chromatids when duplicated |
| Genes | Hereditary information (DNA) passed down from parents |
| Chromatin | DNA wrapped around proteins called histones |
| Somatic Cells | Cells that aren’t gametes; replicate through mitosis |
| Gametes | Sex/germ cells; replicate through meiosis |
| Sister chromatids | Duplicated chromosomes held together by a centromere |
| Centromere | The “narrowed waist” that holds the sister chromatids together |
| Mitosis | Process of cell division |
| Cytokinesis | Division of the cytoplasm |
| How many chromosomes does each somatic cell in our body house? | 46 (2n) |
| How do we inherit our chromosomes? | We receive half from each parent (n) |
| How many chromosomes does a gamete contain? | 23 (n) |
| What is identical between sister chromatids? | Everything; they are genetically identical |
| Where are they attached to each other and what macromolecule facilitates that attachment? | They are attached at the centromere |
| When do sister chromatids become individual chromosomes? | Anaphase (Mitosis) Anaphase II (Meiosis) |
| Does mitosis continue to occur in the human body after birth? If so, in what situation? | Yes, to repair/replace cells and for growth |
| Which phase of the cell cycle is the longest? | Interphase |
| What are the sub-phases of the M phase? Sub-phases of interphase? | M-Phases: Prophase, Metaphase, Anaphase, Telophase Interphase: G1, S, G2 |
| Describe what is happening during the sub-phases of interphase. | G1: Cell prepares to divide through growth and protein and enzyme synthesis S: DNA and organelles duplicated G2: Cytoplasm grows in preparation for division, final checkpoint in interphase before mitosis |
| How many chromosomes are present in a cell in G1 phase? G2 phase? | G1: 46 G2: 46 (92 chromatids) Chromosomes counted by centromere |
| How much DNA is present in a cell during G2 phase in relation to G1 phase? | Double the DNA is present in G2 compared to G1 because the DNA along with the organelles were all doubled in S stage |
| Describe prophase | Chromatin becomes visible and forms sister chromatids, mitotic spindles form, nuclear envelope dissolves |
| Describe metaphase | Mitotic spindles attach to the sister chromatids via the kinetochores on the centromeres and line up the chromatids on the metaphase plate |
| Describe anaphase | Lined up sister chromatids are separated and pulled to opposite ends of the cell by the mitotic spindles |
| Describe telophase | Often overlaps with cytokinesis; cell divides by squeezing the cytoplasm to form a cleavage furrow, nuclear envelope reforms, chromosomes uncoil back into chromatin |
| When does the mitotic spindle begin to form? | Prophase |
| What is the mitotic spindle made of? What structures comprise the mitotic spindle? | Made of centrioles, microtubules, and microfilaments |
| When does the mitotic spindle attach to the kinetochores | Metaphase |
| When does the mitotic spindle pull the separated sister chromatids to opposite sides of the cell | Anaphase |
| When does the mitotic spindle dissolve | Telophase |
| Describe the “tug-of-war” that goes on during metaphase. What is the name of the imaginary plane that the chromosomes align at? | The mitotic spindles attach to the chromosomes and line them up on the metaphase plate |
| What event starts anaphase? | The breaking of the protein cohesion that was holding the sister chromatids together |
| What role do the non-kinetochore microtubules play during anaphase? | The non-kinetochore microtubules get longer, which lengthens the whole cell |
| Describe the process that results in cytokinesis in animal cells. How is this different that the process in plant cells? | Animal cells make a cleavage furrow to start dividing; plants make a cell plate |
| Allele | A type of a gene (Ex: blue eyes or hazel eyes) |
| What are the differences between gametes and somatic cells? | Gametes are sex cells that replicate through meiosis; somatic cells cover the rest of the body and replicate through mitosis |
| Somatic cells are __ ; gametes are __ | diploid; haploid |
| A haploid cell has __ ; a diploid cell has __ | 23 chromosomes (n); 46 chromosomes (2n) |
| Asexual reproduction | Offspring is genetically identical to the parent and is made through mitosis, only one parent is needed |
| Sexual reproduction | Offspring is a genetically random mix of two parents and is produced through meiosis (but once developed grown through mitosis with the exception of the sex cells) |
| Homologous chromosomes | Chromosomes with the same types of genes but not the same specific gene |
| Sex chromosomes | The 23rd pair of chromosomes that are X and Y that determine the human’s sex |
| Autosomes | The first 22 pairs of human chromosomes |
| Diploid cell | Cell with 2 sets of chromosomes (2n; 46 in humans) |
| Haploid cell | Cell with 1 set of chromosomes (n; 23 in humans) |
| Fertilization | Union of haploid sperm and egg cells to form a diploid zygote |
| Zygote | Diploid fertilized egg cell |
| What does the variable n represent when talking about a cell? | Half the number of chromosomes |
| If 2n=8, how many chromosomes would a diploid and haploid cell have? | Diploid: 8 Haploid: 4 |
| If 2n=8, how many homologous pairs of chromosomes would a diploid and haploid cell have? | Diploid: 4 Haploid: 2 |
| A how many chromosomes is a human somatic cell supposed to have? | 46 chromosomes |
| How many chromosomes is a human gamete cell supposed to have? | 23 chromosomes (to make 46 when combined) |
| How many chromosomes is a human zygote cell supposed to have? | 46 chromosomes (half from sperm, half from egg) |
| Meiosis reduces chromosome numbers by half, what process restores chromosome numbers? | Fertilization |
| What are the similarities between mitosis and meiosis? | They take place in the nuclei Result in cell division Occur in the M-phase of the cell cycle Involve DNA synthesis Same names for the stages (PMAT) |
| What are the major events that happen in meiosis that do not occur in mitosis? | Crossing over Double replication (creation of 4 cells) Creation of haploid cells |
| Separation of sister chromatids (meiosis) occurs in | Anaphase II |
| Crossing over occurs in | Prophase I |
| Independent assortment occurs in | Metaphase I |
| What type of cell begins meiosis? | A diploid cell |
| What type and how many cells do we get out of meiosis? | Four haploid cells |
| Define crossing over | When homologous pairs of chromosomes swap parts of their DNA |
| What three things lead to genetic variation in humans? | Independent assortment Random fertilization Crossing over of chromosomes |
| Crossing over of chromosomes occurs in | Prophase I |
| Independent assortment (random pairing of chromosomes) occurs in | Metaphase I |
| Random fertilization occurs | after meiosis |
| Why is genetic diversity important? | It allows more resistance, adaptability, and variation in a species |
| What microorganisms were Hershey and Chase working with? | Bacteriophage (a type of virus) and E. coli |
| What question were Hershey and Chase trying to answer? | Whether DNA or Proteins were the genetic material |
| What DNA and protein characteristics did they use to set up their experiment? | They used radioactive Sulfur (found in proteins but not DNA) and radioactive Phosphorus (found in DNA but not proteins) |
| Would their experiment have worked if they used radio labeled Nitrogen? Why or why not? | No because Nitrogen is found in both DNA and proteins |
| What did Hershey and Chase observe? | That the material the virus injected into the E. coli was marked by the radioactive Phosphorus |
| What conclusion can be made from Hershey and Chase's experiment? | That DNA is the genetic material |
| What are Chargaff's two rules? | Every species differs in its base composition For every A, there is a T. For every C, there is a G |
| The three theories of DNA replication | Conservative Semiconservative Dispersive |
| Conservative | The original DNA helix remained untouched during replication and a 2nd identical helix was created separately |
| Semiconservative | The original helix would separate its DNA strands, and each strand would then be used as a physical template for creating a new, complementary DNA strand. The new helix would be a mix of “old” DNA and “new” DNA |
| Dispersive | The original DNA helix is fragmented and the small pieces serve as a guide for the creation of duplicate pieces, then the fragments somehow reassemble into two new, complete helices |
| How did Meselson and Stahl set up their experiment? | They grew E. coli in N15 (heavier) and N14 (lighter) and placed the N15 E. coli into the N14 E. coli and watched the DNA replicate |
| What did Meselson and Stahl see after 1 round of replication? | 100% were heavy Nitrogen DNA |
| What did Meselson and Stahl see after 2 rounds of replication? | 50% were heavy Nitrogen DNA and 50% were hybrid heavy and light Nitrogen DNA |
| Which theory did Meselson and Stahl’s data support? | Semiconservative DNA replication |
| Origin of replication | place where replication begins |
| Antiparallel | The two DNA strands run opposite to each other |
| 5’ -> 3’ | The direction in which DNA is synthesized 5 carbon sugar to three carbon sugar in the DNA’s backbone |
| Replication fork | The "path" that opens once DNA is unzipped; the two separate open strands the branched DNA at either end of the replication bubble, where new strands are synthesized |
| Leading strand | The top strand that runs 5' -> 3' ; synthesized continuously |
| Lagging strand | The bottom strand that runs 3' -> 5' ; synthesized in fragments by DNA polymerase |
| Okazaki fragment | The fragments that are made when DNA is synthesized on the lagging strand |
| Why does DNA replication only proceed from 5’ -> 3’? | Necessary for repair and energy |
| What steps are needed to fix the lagging strand after it has been made? | RNA primers replaced with DNA and gaps are sealed by ligase |
| Enzymes involved in DNA replication | Primase Helicase DNA polymerase I DNA polymerase III Ligase Topoisomerase Single-strand binding proteins |
| Function of primase | sets down RNA primers to show DNA polymerase where to build DNA |
| Function of helicase | breaks the hydrogen bonds between the DNA bases to 'unzip' the DNA and separate the two helices |
| Function of ligase | Seals the gaps of DNA on the lagging strand after the RNA primers are replaced with DNA |
| Function of topisomerase | Relaxes the DNA strands to keep it from snapping it back together |
| DNA polymerase builds new DNA in | the 5' -> 3' direction |
| Result of DNA replication | 2 DNA molecules, each made of 1 old strand and 1 new strand |
| SSB (single-strand binding) proteins | Hold on to the DNA to keep it from snapping back together |
| Function of DNA polymerase I | Removes RNA nucleotides from the lagging strand and replaces them with DNA |
| Function of DNA polymerase III | Adds DNA to and RNA or pre-existing DNA strand using the old DNA as a template |
| The genetic code is | Redundant Unambiguous Nearly universal Without punctuation |
| one gene–one polypeptide hypothesis recognizes that | some proteins are composed of multiple polypeptides |
| Steps of gene expression | Transcription Translation DNA -> RNA -> proteins |
| What is the genetic code? | the instructions contained in a gene that tell a cell how to make a specific protein |
| What is a codon? Why must a codon be three nucleotides and not one or two? | A codon is a combination of three nucleotides; must be three so there can be enough variety in combinations to have at least one combination for every amino acid |
| How many possible codons exist? How many amino acids? | 64 possible codons for 20 amino acids |
| The DNA strand is the ___ of the mRNA strand | opposite |
| What is the process of transcription? | DNA unzips section RNA polymerase moves down the DNA and makes a copy into mRNA RNA polymerase leaves mRNA left behind and DNA zips back together |
| What enzyme is responsible for carrying out transcription? | RNA polymerase |
| How does the cell know where to begin transcription and where to end transcription? | It starts at the promoter sequence and ends at the terminator sequence |
| What is the process of translation? | The synthesis of proteins under the direction of mRNA |
| What is responsible for carrying out translation? | tRNA |
| Role of tRNA in translation | transfer amino acids from the cytoplasm to the ribosomes for the amino acids to attach to each other and form a polypeptide chain (protein monomer) |
| Role of mRNA in translation | delivers the translated DNA for the tRNA and ribosomes to bond to in order |
| Role of rRNA in translation | Reads the codons and signals for the right tRNA to make the right protein |
| Role of the anticodon in tRNA | allows tRNA to bind to the codon on the mRNA and signal for a specific amino acid |
| Why is it so important that the anticodon and amino acid of a tRNA match according to the genetic code? | If not they could bring the wrong amino acid, which could be disastrous |
| A ribosome is made up of the following sites | P site and A site |
| Function of the P site in a ribosome | The site where the first tRNA binds to |
| Function of the A site in a ribosome | The site where all the other tRNA bind to |
| What happens during translation | mRNA arrives at ribosome Ribosome reads mRNA codons Codons call for specific tRNA with amino acids to make a specific protein Ribosome reads stop codon and stops production |
| Missense mutation | Change in a nucleotide that changes the codon to code for a different amino acid than intended |
| Nonsense mutation | A change in base causes a stop codon to be present prematurely, halting the protein creation sequence |
| Silent mutation | Just one letter changes; does not affect protein formation |
| Frameshift mutation | Insertion or deletion; could shift all the codons after possibly creating totally different proteins with possibly disastrous results |