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Norman Borlaug's contribution to the Green Revolution and its significance
He helped lead the GR by developing high-yield, disease-resistant wheat. His work increased food production and helped prevent famine for an est. one billion people.
Structures/organelles unique to an animal cell
No cell wall, no chloroplast, no large central vacuole
Structures/organelles unique to a plant cell
Has cell wall, chloroplasts, and a large central vacuole
Structures/organelles unique to a prokaryotic cell
No nucleus, no membrane-bound organelles, pro=simple
Nucleus
The control center of a eukaryotic cell. It stores DNA and controls gene expression.
Nuclear envelope
Surrounds nucleus; controls what enters/exits
Nucleoplasm
Fluid inside the nucleus
Chromatin
DNA + proteins; contains genes
Nucleolus
Makes rRNA and assembles ribosomal subunits
How does the nucleus regulate genes?
Controls which genes are turned on/off through chromatin organization
Where does transcription occur?
Nucleus
What happens during RNA processing?
5' cap, intron removal, exon joining, poly-A tail
What does the nucleus do during cell division?
Replicates and organizes DNA so chromosomes are properly distributed
Chromatids
Two identical copies of a chromosome joined together after DNA replication
Centromere
CENTRO= center; a region that holds sister chromatids together; spindle fibers attach here
Telomere
TELO= ends; protective ends of chromosomes; prevent DNA damage/loss
Euchromatin
EU= Easy to access; access; loosely packed DNA; genes are usually active/expressed
Heterochromatin
HETERO= Hidden; tightly packed DNA; genes are usually inactive/not expressed
Metacentric
META= Middle; centromere is in the middle; arms are about equal
Acrocentric
ACRO= Almost end; centromere is near one end; one short arm and one long arm
Telocentric
TELO= Totally end; centromere is at the very end; one arm
Gene
Segment of DNA at a specific locus that codes for a trait
Allele
Alternative version of a gene at that same locus
Locus
Location of a gene on a chromosome
Genotype
The specific allele combination an organism carries (e.g. Gg)
Phenotype
The observable trait that results (e.g. green seed color)
Homozygous
Two identical alleles at a locus (GG or gg)
Heterozygous
Two different alleles at a locus (Gg)
Haploid (n)
One set of chromosomes; found in gametes (sperm/egg)
Diploid (2n)
Two sets of chromosomes; one set from each parent
Corn's haploid (n)/diploid (2n) number
(n)=10 chromosomes (2n)=20 chromosomes
Interphase
Prepares cell for mitosis
G1 phase
Cell grows and performs normal functions
S phase
DNA is duplicated
G2 phase
Cell grows more and prepares for cell division
M phase
Mitosis + cytokinesis: nucleus divides, then cells split
Sister chromatids: how and when they form
One chromosome copies its DNA and forms during the S phase of interphase
PMAT
Prophase, Metaphase, Anaphase, Telophase
Prophase
Chromosomes condense, nuclear envelope breaks down, and spindle fibers form
Metaphase
Chromosomes line up in the middle of the cell
Anaphase
Sister chromatids separate and move to opposite sides
Telophase
Two new nuclei form around chromosomes and begin to uncoil
Genetic significance of mitosis
It produces two genetically identical daughter cells
How does mitosis maintain genetic material?
DNA is copied before mitosis, then sister chromatids are separated equally between the two daughter cells
Why does meiosis produce haploid and genetically variable cells, unlike mitosis?
Meiosis has two divisions, reducing chromosome number to haploid (n), and creates genetic variation through crossing over and independent assortment
Meiosis I
Reductional division: separates homologous chromosomes; produces 2 haploid cells
Prophase I
Homologous chromosomes pair up; crossing over occurs
Metaphase I
Homologous pairs line up in the middle
Anaphase I
Homologous chromosomes separate
Telophase I
Two haploid cells form
Meisosis II
Equatorial division: separates sister chromatids; produces 4 haploid cells
Prophase II
Spindle forms; chromosomes condense
Metaphase II
Chromosomes line up in the middle
Anaphase II
Sister chromatids separate
Telophase II
Four haploid cells form
LZPDD
Leptotene, Zygotene, Pachytene, Diplotene, Diakinesis
Leptonema (Leptotene)
Chromosomes condense into long, thin visible threads
Zygonema (Zygotene)
Synapsis occurs; homologous chromosomes pair
Pachynema (Pachytene)
Crossing-over occurs; bivalents shorten and thicken as synapsis completes, exchanging DNA and creating genetic variation
Diplonema (Diplotene)
Homologs start to pull apart, but chiasmata remain
Diakinesis
Chromosomes condense further; nuclear envelope and nucleolus break down
Synaptonemal complex
A protein/DNA scaffold; holds homologs together
Bivalent
Paired set of homologous chromosomes (4 chromatids total)
Chiasma (plural: chiasmata)
X-shaped point where two chromatids physically cross
Crossing-over
Non-sister chromatids exchange segments
Recombinant chromosome
Chromosome containing a new combination of alleles created by crossing-over
Genetic recombination
Creation of new combinations of genetic material, increasing genetic variation
Why is meiosis important?
Maintains chromosome number and creates genetic diversity through independent assortment and crossing-over
Mendel's three postulates that explain transmission genetics
Segregation, independent assortment, and dominance
Segregation
Paired factors segregate during gamete formation at random, so each gamete recieves only one form
Indepdent Assortment
When two or more trait pairs are considered together, each pair assort into gametes independently of the others
Dominance
One trait is expressed to the exclusion of the alternative trait present in one of the parents
Qualitative
Distinct categories (e.g. flower color)
Quantitative
Measurable values with continuous variation (e.g. height, weight)
Monohybrid cross (Aa x Aa)
3:1 phenotype, 1:2:1 genotype
Dihybrid cross (AaBb x AaBb)
9:3:3:1 phenotype
Linkage
Certain genes tend to be inherited together
Complete linkage
Genes are very close together on the same chromosome and are inherited together; no crossing-over occurs between them
Incomplete linkage
Genes are on the same chromosome, but crossing-over can separate them, producing recombinant offspring
Coupling (cis)
One chromosome carries both dominant alleles (AB), the other both recessive (ab)
Repulsion (trans)
One chromosome carries one of each (Ab), the other the opposite (aB)
Chi-Square Test
Χ² = Σ (O − E)² / E
If calculated Χ² is below the critical value: the data is consistent with your expected ratio
If calculated Χ² exceeds the critical value: something (often linkage) is skewing the ratio
Incomplete dominance + F1/F2 outcomes
The heterozygote shows a phenotype intermediate between the two homozygotes (blended; red + white = pink)
F1: 100% intermediate
F2: 1:2:1 phenotype + genotype
Codominance + F1/F2 outcomes
Both alleles in a heterozygote are fully expressed
F1: 100% both traits expressed
F2: 1:2:1 phenotype + genotype
How does zygosity determine predictable breeding outcomes (e.g. roan horse coat color)
The roan coat color is incomplete dominance, so the heterozygous has its own distinct phenotype
Oligogenic inheritance
OLIGO=few, a trait that is controlled by a few genes
Polygenic inheritance
POLY=many, a trait that is controlled by many genes, often producing continuous variation
Epistasis
When one gene affects or masks the expression of another gene
Complementary action
(work together) Two genes both required for one effect
Modifying action
(changes) One gene's effect depends on another
Inhibiting action
(stops) One gene blocks a second gene's effect
Masking action
(hides) One gene hides a second gene's effect
Duplicate action
(each do the same thing) Either gene alone produces the same effect
Additive action
(add up) Two genes' effects combine when both present
Pleiotropic effect
One gene affecting multiple traits
Similarities between DNA and RNA
Both are nucleic acids made of nucleotides and contain genetic information
DNA
Deoxyribose sugar, A-T-C-G, double-stranded, stores genetic information
RNA
Ribose sugar, A-U-C-G, single-stranded, helps make proteins and regulate genes
C-value
The amount of DNA in one haploid genome
C-value paradox
That correspondence is not reliable—genome size does not track complexity