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mitosis
cell division that results in two daughter cells each having the same number and kind of chromosomes
starting cell in mitosis (diploid cell) 2n
mitosis phases
prophase
metaphase
anaphase
telophase
cytokinesis
prophase
chromosomes become visible as they condense and thicken
metaphase
chromosomes align in the cell’s center, forming a single row
anaphase
chromatids are separated and drawn to the opposite ends of the cell by spindle fibers
telophase
chromosomes reach the opposite sides of the cell, forming new nuclear envelopes around the chromosomes
cytokinesis
splits the cytoplasm of the cell, two identical diploid
meiosis
cell division that results in four daughter cells each with half the number of chromosomes of the parent cell
starting in cell meiosis (diploid cell) 2n
primary spermatocyte
primary oocyte
meiosis phases
prophase 1&2
metaphase 1&2
anaphase 1&2
telophase1&2
cytokinesis 1&2
prophase 1
chromosome condensation and pairing of homologous chromosomes
metaphase 1
chromosomes align in the middle of the cell’s center, maintaining their homologous pairs
anaphase 1
chromosomes are separated and drawn to the opposite ends of the cell by spindle fibers
telophase 1
chromosomes reach the opposite sides of the cell, forming new nuclear envelopes around the chromosomes
cytokinesis 1
splits the cytoplasm of the cell
prophase 2
chromosome condensation in both cells
metaphase 2
chromosome align in the middle of the cell’s center, forming a single row
anaphase 2
chromatids are separated and drawn to the opposite ends of the cell by spindle fibers
telophase 2
chromosomes reach the opposite sides of the cell, forming new nuclear envelopes around the chromosomes
cytokinesis 2
splits the cytoplasm of the cell
four non-identical cells (gametes)
haploid cells: 2 groups of 23 chromosomes
heredity
the passing on of physical or mental characteristics genetically from one generation to another
height, eye color, risk for certain diseases, hair color
DNA
self-replicating material that is present in nearly all living organisms as the main constituent of chromosomes
deoxyribonucleic acid - double helix shaped
nucleotide
held together by hydrogen bonds
phosphate, deoxyribose (a sugar), nitrogenous bases (code for traits)
adenine to thymine
cytosine to guanine
genes
a unit of heredity which is transferred from a parent to offspring and is held to determine some characteristics of the offspring
protein can code for genes
structural genes
eye/hair color, transport, structure, enzymatic activity, defense mechanisms, etc
regulatory genes
used to control the timing, location and amount in which genes are expressed
genes can be activated and deactivated through various mechanisms
chromosomes
a threadlike structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form of genes
made up of DNA
humans have 46 chromosomes (23 from mom and 23 from dad)
RNA
a nucleic acid present in all living cells whose principal role is to act as a messenger carrying instructions from DNA for controlling synthesis of proteins
ribonucleic acid, single strand
different sugar base
adenine to uracil
cytosine to guanine
mRNA
carries genetic information to make proteins
rRNA
serve as a location for protein synthesis
tRNA
an adaptor molecule that decodes an mRNA into a protein
transcription
process of making an RNA copy of a gene’s DNA sequence
RNA polymerase connects complementary RNA bases to the DNA
translation
process of translating the sequence of a mRNA to amino acids during protein synthesis
transcription → translation
forms single strand of mRNA → strand gets sent to ribosomes (rRNA) → translates sequence from mRNA during protein synthesis (tRNA)