Ch. 2: Reproduction Flashcards
Diploid (2n)
Type of cell, has 2 copies of each chromosome, autosomal cells
Haploid
Type of cell, has 1 copy of each chromosome, germ cells
Cell Cycle: Interphase
G1, S, G2, DNA is uncoiled into the form of chromatin in this phase, longest part of cell cycle, even actively dividing cells spend 90% of their time in interphase
G1
Presynthetic gap, cells create organelles (mitochondria, ribosomes, and endoplasmic reticulum) for energy and protein production while also increasing their size. There is a restriction point where DNA is checked for quality to move onto S stage, if there is damage to DNA, cell cycle goes into arrest until DNA has been repaired
S
Synthesis, DNA is replicated, the 2 strands of DNA called chromatids are held together @ centromere w cohesin
G2
Postsynthetic gap, there is further cell growth and replication of organelles in preparation for mitosis, cell checks if there are enough organelles and cytoplasm for 2 daughter cells another quality checkpoint must be passed to go to mitosis (not sure if this is part of G2)
M
Mitosis, mitosis and cytokinesis occur: prophase, metaphase, anaphase and telophase
G0
The cell performs its function without any preparation for division
P53
Protein that plays a role in the 2 major checkpoints of the cell cycle (G1 to S and G2 to M)
Cyclins and Cyclin Dependent Kinases (CDKs)
Concentrations rise and fall during the cell cycle, diff types of Cyclins bind to CDKs, phosphorylating and activating transcription factors for the next stage of the cell cycle
Transcription factors
Promote transcription of genes required for the next step of the cell cycle
Cancer
Occurs when cell cycle control becomes deranged, allowing damaged cells to undergo mitosis without regard to quality or quantity of the new cells produced. Cancerous cells may begin to produce factors that allow them to escape their site and invade or metastasize elsewhere. One of the most common mutations is one where gene which produces p53 is mutated and produces TP53
Somatic cells
Undergo mitosis to form 2 genetically identical diploid daughter cells from a single cell
4 phases of Mitosis
- Prophase: chromosomes condense, nuclear membrane dissolves, nucleoli disappear, centrioles migrate to opposite sides of the cell, and the spindle apparatus (defines plane of division) begins to form. The kinetochore of each chromosome is contacted by a spindle fiber
- Metaphase: chromosomes line up along the metaphase plate (equatorial plate)
- Anaphase: sister chromatids are separated and pulled to opposite poles
- Telophase: nuclear membrane reforms, spindle apparatus disappears and cytosol and organelles are split between the two daughter cells through cytokinesis
Meiosis
Occurs in gametocytes (germ cells) and produces up to 4 non-identical haploid sex cells (gametes)
- 1 round of replication and 2 rounds of division
Meiosis I
Homologous pairs of chromosomes (homologues) are separated from each other. Homologues are chromosomes that are given the same number but are of opposite parental origin
- Prophase I: same as prophase in mitosis except homologues come together and intertwine in a process called synapsis. The 4 chromatids are referred to as a tetrad and crossing over exchanges genetic material from one chromatid w material from a chromatid in the homologous chromosome (Mendel’s second law– independent assortment)
- Metaphase I: homologous chromosomes line up on opposite sides of the metaphase plate
- Anaphase I: homologous chromosomes are segregated to opposite poles of the cell. (Mendel’s first law– segregation)
- Telophase I: the chromosomes may or may not fully decondense, and the cell may enter interkinesis after cytokinesis
Meiosis II
Sister chromatids are separated from each other in a process that is functionally identical to mitosis
- Sister chromatids are copies of the same DNA held together @ the centromere
What is biological sex determined by?
23rd pair of chromosomes in humans
XX is female and XY is male
X chromosome
- carries sizable amt of genetic info
- mutations of X-linked genes can cause sex-linked disorders
Hemizygous
- males have only 1 X chromosome so they will express sex-linked disorders, even if they only have one recessive disease-carrying allele
- women w one copy of the affected allele are called carriers
Y chromosome
Carries little genetic info, but contains the SRY (sex-determining region Y) gene which causes the gonads to differentiate into testes which have 2 fuctional components: seminiferous tubules and interstitial cells of Leydig
Male Reproductive System:
Contains both internal and external structures
Sperm
- develop in the seminiferous tubules in the testes
- nourished by Sertoli cells