1/20
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
Gene
unit of hereditary transferred from parent to offspring — small region of chromosome that encodes a specific protein
hershey + chase showed DNA contains genetic info
DNA
made of nucleotide units: phosphate grp (outer circle), deoxyribose (hexagon), nitrogenous base
purine: A, G - double ring
pyrimidine: C, T, U - single ring
double helix, 5’ to 3’ each strand
hydrogen bonds hold bases together
RNA
single stranded copy of DNA that carries genetic info
mRNA: (messenger) transcribed in nucleus and leaves to cytoplasm to bring info
rRNA: (ribosomal) makes up ribosomes
tRNA: (transfer) brings amino acids during translation
Transcription
making RNA copies in nucleus
1) initiation - RNA polymerase binds to promoter at start of gene and unzips DNA
2) elongation - RNA polymerase moves along copying RNA from DNA and joins complimentary bases together to form 3’ to 5’ RNA
3) Termination - at terminator sequence on DNA, all units separate and DNA winds into helix again
RNA processing
must happen after transcription before translation in order for mRNA to leave nucleus
cap is added to 5’ end, poly-A tail added to 3’ end
introns (not used to produce protein) are removed leaving only exons
Translation
making proteins in cytoplasm (multiple ribosome units attach to each exon to be efficient)
1) initiation - small ribosomal subunit binds to mRNA followed by large subunit. Initiator tRNA binds already containing base pairs and amino acid (anticodon matches up with START codon = MET amino acid)
2) elongation - second tRNA enters ribosome where its anticodon matches second mRNA codon and amino acids joined together by enzymes forming a peptide bond. tRNA leaves and amino acid stays in chain
3) Termination - at stop codon, release factor protein binds causing polypeptide to release where it will fold into functional protein
Gene regulation
highly regulated - requires lots of energy
prokaryotes: genes organized as operons (grps of genes always transcribed together) which contain promotors (initiate), operators (affect activity of RNA polymerase), and repressors (end)
Eukaryotes:
transcription factors: proteins that bind to gene to affect RNA polymerase activity (transcription only occurs if factors are correct)
alternate splicing: creates different proteins from same mRNA by rearranging exons
Mutations
changes in DNA sequences that are not always harmful
point mutation: changes one or few base pairs
frameshift mutation: insertion or deletion of nucleotide
DNA replication
1) helicase unwinds DNA (many origins) and single-strand binding proteins hold parent strands apart
2) primase adds short strand of RNA to each template (lagging strand needs more)
3) DNA polymerase adds nucleotides using RNA primer to create daughter strands (leading strand has one continuous)
4) ligases remove primer and form covalent bonds btwn DNA
Binary Fission
prokaryotes asexually replicate DNA to two identical daughter cells
singular chromosome is replicated and each attach to opposite ends of cell and divides
DNA condensation
DNA condenses into chromosomes before division but is usually loose otherwise
nucleosomes: loose DNA wraps around histones
chromatin: nucleosomes coil tighter into thick string
chromosomes: chromatin coils into X shapes
Cell cycle
Interphase: phase of cell that replicates DNA and carries out necessary functions
G1: normal cell function + growth
G0: cell most of the time
S: cell replicates entire genome
G2: additional growth for mitosis
Cell division
Mitosis: cells leave G2 and enter cell division phase
1) prophase: chromosomes + spindles form
2) prometaphase: chromosomes attach to spindle fibers
3) metaphase: chromosomes line up in center
4) anaphase: chromatids separate
5) telophase: two nuclei form around chromosomes
cell proceeds to cytokinesis:
cleavage furrow: deepening ring of protein beneath cell membrane for cell to split
Checkpoints
ensure that DNA is replicated properly and is not damaged, and that chromosomes line up and separate properly
if checkpoints fail, causes cancer cells: have distinct features - lose specialization, divide endlessly, can regenerate end of chromosome
apoptosis: programmed cell death if cell does not meet requirements
Asexual vs sexual reproduction
asexual reproduction: one parent replicates DNA and splits into two genetically identical offspring (bacteria, archaea, protists)
sexual reproduction: DNA of offspring comes from two parents - egg fuses with sperm to create genetically diverse offspring to increase chance some will survive in changing environments
diploid cells
diploid cell: two sets of chromosomes from each parent - human cells contain 23 sets of chromosomes (22 autosomes + 1 sex)
homologous pair: chromosomes similar in size and structure and carry same sets of genes (even if different alleles)
Haploid cells
haploid cell: one set of chromosomes (gametes)
zygote: when two haploid sperm + egg cells fuse - first new cell of organism
germ cells: in adults, these cells divide by meiosis to form haploid gametes
Meiosis
DNA replicates one, but nucleus divides twice - contains half as many chromosomes
1) prohase 1: homologous chromosomes pari up and attach to spindle
2) metaphase 1: homologous chromosomes line up in middle
3) anaphase 1: chromosomes seperate
4) telophase 1: nucleus forms
cytokinesis occurs
5) prophase 2: chromosomes attach to spindle
6) metaphase 2: chromosomes line up in middle
7) anaphase 2: chromaTIDS seperate
8) telophase 2: nucleus forms
cytokinesis occurs
4 total new cells created
increasing genetic variability
crossing over: occurs in chiasma during prophase 1 - two homologous chromosomes pair up and exchange a piece each
independent assortment: during metaphase 1, germ cell with 3 chromosome pairs has 4 possibel arrangements = 8 possible gametes
twins
monozygotic twins: genetically identical - embryo splits
dizygotic twins: two separate sperm with two separate egg cells
nondisjunction
chromosome fails to separate properly in anaphase 1 or 2 and can kill the whole cell
down syndrome is caused by 3 copies of chromosome #21