Biology Of Cell Flashcards
Describe the structure of nucleic acids including base pairing and covalent vs hydrogen bonds.
Each nucleic acid includes Sugar, phosphate, nitrogenous base, hydrogen bond
Compare and contrast DNA and RNA structure.
DNA: Made up of nucleotides, Uses Thymine, double-stranded, nucleus only
RNA: Made out of nucleotides, has 2 hydroxyl groups, uses uracil, single-stranded, nucleus and cytoplasm
Define the following terms: chromosome, histone, homologous chromosome, centromere, sister chromatid, telomeres, diploid, haploid, gene, genetic locus, allele and genome.
Chromosome: DNA associated with an array of different proteins into a complex structure
Histone: Proteins that compact DNA to fit into the cell
Homologous chromosome: Two versions of each chromosome
Centromere: Where the chromatids get stuck
Sister Chromatid: two identical copies of the same chromosome formed by DNA replication
Telomeres: Protect functional genes from worn-down damage
Diploid: two complete sets of chromosomes
Haploid: Gametes/Sex cells, contain unpair chromosomes
Gene: Specific stretch of DNA that codes for protein
genetic locus: Specific location on the chromosome
Allele: One copy for the opposite of the other
Genome: The complete complement of genetic material in an organism
Describe the basic process of DNA replication and how it leads to the creation of identical sister chromatids.
Parents molecules: strands are together and have 1 chromosome and 1 chromatid
Separation of Strands: the parent strands start to separate
Daughter cells: Makes a copy of each strand then gets paired with a new strand “one old and one new”
Outline the events of each stage (G1, S, G2, M) of the cell cycle. Indicate which stage the majority of cells are in, when chromosomes replicate (DNA replication), when chromosomes segregate, and when the cell divides.
G1: Active gene expression, Preps DNA synthesis
S: DNA synthesis, creates identical sisters for each chromosome
G2: Prep for Cell Division
M: Cell division
Describe what main action happens in each of the following stages of mitosis: Prophase (3 actions), Metaphase, Anaphase and Telophase (3 actions).
Prophase: Dissolves nuclear membrane, co-dense DNA, Mitotic spindle forms
Metaphase: Nuclear membrane reforms, DNA unwinds/deco-dense, Mitotic spindle breaks down
Anaphase/Telophase: Two daughters produce by mitosis
Explain the role of meiosis in the diploid life cycle, including the terms gametes, somatic cells, and germ cells.
Meiosis produces haploid gametes from diploid germ cells, which are used in sexual reproduction to form a new diploid organism. Somatic cells are diploid and undergo mitosis for growth and maintenance of the body.
Describe the primary similarities and differences between mitosis and meiosis.
Mitosis and meiosis are two types of cell division processes. Mitosis results in two identical daughter cells, while meiosis produces four genetically diverse daughter cells due to chromosome pairing and recombination. Mitosis involves one cell division, while meiosis involves two rounds of cell division. Mitosis is involved in growth, repair, and asexual reproduction, while meiosis is involved in sexual reproduction and creating genetically diverse offspring.
Define dominant and recessive phenotypes, and describe how each corresponds with homozygous and/or heterozygous genotypes.
Dominant traits are expressed if an organism inherits one or two copies of the gene responsible for the trait.
Recessive traits are only expressed if an organism inherits two copies of the gene responsible for the trait.
Homozygous dominant and heterozygous genotypes are usually associated with dominant traits, while homozygous recessive genotypes are associated with recessive traits.
Identify Huntington’s disease and familial hypercholesterolemia as prevalent autosomal dominant human disorders, and identify cystic fibrosis and sickle cell anemia as prevalent autosomal recessive disorders.
Huntington’s disease and familial hypercholesterolemia are autosomal dominant disorders
Cystic fibrosis and sickle cell anemia are autosomal recessive disorders.
Huntington’s disease affects brain function, familial hypercholesterolemia causes high cholesterol, cystic fibrosis affects the lungs and other organs, and sickle cell anemia causes blood disorders.
Define the terms gene expression, transcription, and translation.
Transcription: The process of using a DNA template to make mRNA
Translation: Process of making a polypeptide using mRNA template
Explain the basic steps of transcription (initiation, elongation, termination).
Initiation: mRNA and ribosome segments come together. tRNA carrying the first amino acid binds to the start codon
Elongation: Amino acids are carried by tRNA to the mRNA. They create a long polypeptide chain
Termination: The stop codon in mRNA is found by the release factor, a protein, and translation components come apart. This releases the polypeptide chain
Explain the basic steps of translation (initiation, elongation, termination).
Initiation: RNA polymerase binds to the promotor region of the gene
Elongation: RNA polymerase slides along the region of the gene that gets transcribed, matching RNA nucleotide to DNA template
Termination: RNA polymerase hits the terminator region of gene and detaches from DNA
Explain how the triplet code works. Be able to build an amino acid chain from an mRNA sequence, if given the codon chart.
The bases in mRNA are read in triplets, Start codon is AUG and stops at UAA, UAG, UGA
Explain how DNA mutations can arise and describe different types (point, insertion, deletion) of mutations.
Point: Change in a single nucleotide base pair
Insertion: Addition of one or more nucleotides
Deletion: Removal of one or more nucleotide