what type of cells does mitosis occur?
Somatic
Site of replication is called
Origin of replication
What molecule carries amino acids to the ribosome during translation?
tRNA
What is the mutagen used in your activity
UV- Ultraviolet
Father of Genetics
gregor mendel
Identify the stage of mitosis.
Prophase
What base in RNA pairs with adenine in DNA?
In RNA, uracil (U) pairs with adenine (A).
If the Anti-codon is ACC what is the mRNA codon
UGG
What type of Mutagen is induced in the activity?
Physical
In a dihybrid cross of two heterozygous individuals (AaBb × AaBb), what is the classic phenotypic ratio?
9:3:3:1 ratio
In what stage of meiosis does crossing-over occur, and why is it important?
Crossing-over occurs in Prophase I of meiosis; it increases genetic variation by recombining alleles.
What do you call the strand that is being transcribed?
name the 3 terms
Template Strand
Non-coding Strand
Antisense Strand
Name the 3 sites of the ribosome
A-aminoacyl site
P-Peptidyl site
E-exit site
Differentiate between somatic and germline mutations in terms of their effects on evolution and inheritance.
Somatic mutations: Affect only body cells, not inherited (may cause cancer).
Germline mutations: Passed on to offspring, fuel evolution.
If a lethal gene is homozygous YY what percent or ratio is affected in the crossbreed of BBYY x bbyy
none or 0 percent
Compare the outcomes of mitosis and meiosis in terms of chromosome number and genetic variation.
Mitosis: Produces 2 diploid identical cells (2n), no genetic variation.
Meiosis: Produces 4 haploid cells (n), each genetically unique.
what is the function of the TATA box and what type of organisms can it be found in?
promoter regions for eukaryotes
what are the 3 stop codons
UAA, UAG, and UGA
what factor besides the mutagen induced in the seeds affects the potential growth in the activity.
exposure duration: Longer exposure increases the number of mutations, making DNA repair mechanisms insufficient → more severe phenotypic abnormalities and lower survival rates.
What is the Phenotype ratio or percent if you crossbreed BBxxZZyy x bbXXzzYY
1 or 100% BbXxZzYy
Illustrate or explain how nondisjunction during meiosis I can lead to aneuploidy. Provide an example of a human disorder caused by this error.
Nondisjunction in Meiosis I → homologous chromosomes fail to separate → gametes with extra or missing chromosomes. Example: Trisomy 21 (Down syndrome).
In order explain the enzymes involved in DNA replication and their functions.
Topoisomerase - Relieves tension and supercoiling ahead of the replication fork by cutting and rejoining DNA strands.
Helicase -Unzips the DNA double helix by breaking the hydrogen bonds
SSBPs- Bind to the separated DNA strands to keep them from reannealing
Primase - Synthesize the RNA primer
DNA Polymerase III - Adds nucleotides to the growing DNA strand in the 5′→3′ direction.
DNA Ligase - joins Okazaki fragments by sealing the sugar-phosphate backbone with phosphodiester bonds.
explain translation elongation
initiation- (tRNA entry An elongation factor brings a new aminoacyl-tRNA into the A site. Peptide bond formation: Peptidyl transferase (part of large ribosomal subunit) forms a bond between amino acids in the P and A sites. Translocation: Ribosome shifts 3 bases along mRNA, moving the tRNA with the polypeptide to the P site, and the empty tRNA to the E site (where it exits). - termination
Explain the scenario if mutations did occur but nothing happens to the plant or seed.
Many mutations are silent/neutral or occur in non-coding regions.
Plants have backup metabolic pathways and efficient DNA repair systems, allowing some individuals to overcome UV-induced damage.
For a child to have AB blood type, one parent must contribute an Ia allele and the other must contribute an Ib allele. What are all the possible combinations of the parent
Parent 1: Type A (IAIA or IAi), Parent 2: Type B (IBIB or IBi)
Parent 1: Type AB (IAIB), Parent 2: Type A (IAi or IAIA)
Parent 1: Type AB (IAIB), Parent 2: Type B (IBi or IBIB)
Parent 1: Type AB, Parent 2: Type AB