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Biology Chapter 4
4A, 4B, 4C, 4D
| Question | Answer |
|---|---|
| Purposes of cell replication | Growth and development , Maintenance and repair, Reproduction |
| binary fission | the method of cell replication used by prokaryotes |
| Exponential growth | Cells replicate exponentially, meaning that after each round of replication the number of cells present doubles. |
| Exponential growth example | the rapid nature of binary fission allows a single bacterium to replicate into a few million bacteria in a very short span of time. A colony of Escherichia coli (E.coli) bacteria doubles in size every 20 minutes |
| Prokaryotes reproduction | reproduce rapidly via binary fission, which produces two genetically identical copies of a cell. (asexual reproduction) |
| different stages of binary fission | D – DNA replication E – Elongation S – Septum formation C – Cell division |
| The process of binary fission pt 1 | The circular chromosome is uncoiled and the DNA is replicated. Plasmids also replicate, , the cell elongates as it prepares to separate into two new cells and the duplicated circular chromosomes migrate to opposite ends. |
| The process of binary fission pt 2 | The cell then begins to undergo cytokinesis – the process of separating into two new cells – by pinching inwards and creating a septum, A new cell wall and membrane are formed down the centre of the cell |
| eukaryotic cell cycle | composed of three stages including interphase, mitosis, and cytokinesis. |
| interphase | the first stage of the eukaryotic cell cycle which involves cellular growth and duplication of chromosomes. Composed of three phases: G1, S, and G2 |
| Interphase processes | the cell synthesises the necessary DNA, proteins, and organelles required for growth and replication |
| Gap 1 (G1) phase | • increasing the volume of its cytosol • synthesising proteins for DNA replication • replicating its organelles. At the end of the G1 phase, the cell either proceeds to the S phase or exits the cell cycle and enters the G0 phase. |
| Gap 0 (G0) phase | Cells that are not required to replicate rest in the G0 phase either quiescent or terminally differentiated. While quiescent cells are dormant and have the ability to re-enter the cell cycle, terminally differentiated cells remain in G0 indefinitely. |
| Synthesis (S) phase | the cell replicates its DNA turning one chromosome into two genetically identical sister chromatids, While sister chromatids are held together by a centromere, the pair is regarded as a single chromosome. |
| Gap 2 (G2) Phase | The G2 phase is the final stage of interphase where the cell continues to grow and prepare itself for mitosis. • increasing the volume of the cytosol • synthesising proteins in preparation for mitosis. |
| Mitosis | second stage of the eukaryotic cell cycle and involves the separation of the newly replicated chromosomes into two new nuclei. (4 substages) |
| Prophase | begins with the condensation chromosomes so that they are visible Simultaneously, the centrioles migrate towards opposite ends (or poles) of the cell, and spindle fibres begin to form. The nuclear membrane breaks down and the nucleolus disappears. |
| Metaphase | , the spindle fibres fully form and attach to the centromere of each chromosome. This allows the spindle fibres to guide the chromosomes towards the equator of the cell where they line up. |
| Anaphase | The spindle fibres contract, splitting the centromere and pulling sister chromatids to opposite ends of the cell. |
| Telophase | new nuclear membranes form, producing two genetically identical nuclei. The spindle fibres disintegrate and the chromosomes decondense. |
| Cytokinesis | the third and final stage of the eukaryotic cell cycle, where the cell divides into two daughter cells. |
| cytokinesis process | the cytoplasm divides and the organelles evenly distribute themselves before separating into two daughter cells. |
| cytokinesis process in animals | occurs when a cleavage furrow develops and pinches the plasma membrane into two cells |
| cytokinesis process in plants | because they have a cell wall, a cell plate first forms at the equator before separating into two cells (vesicles accumalte in the centre of the cell and the cell plate froms along the equator) |
| Regulation of the cell cycle | The cell cycle has three checkpoints where the cell inspects itself for errors before proceeding to the next stage. |
| 3 checkpoints | occur at the end of the G1 and G2 phases, and during metaphase |
| G1 checkpoint | verifies that the cell has grown to the correct size, has synthesised enough protein for DNA replication, checks if the DNA has been damaged during mitosis and cell growth, and checks if there are enough nutrients and oxygen |
| G2 checkpoint | ensures that DNA has replicated properly in the S phase, and that the cell has enough resources for mitosis |
| metaphase checkpoint | the cell checks the formation of the spindle fibres. If the chromosomes are lined up in the correct location, the cell proceeds to anaphase. |
| apoptosis | the controlled death of cells in the body. Also known as programmed cell death |
| two pathways of apoptosis | the mitochondrial and the death receptor pathways |
| Mitochondrial pathway (intrinsic pathway) | the pathway of apoptosis which is initiated by the detection of internal cellular damage. Also known as the intrinsic pathway |
| Mitochondrial pathway (intrinsic pathway) process | When internal components of the cell are damaged mitochondria detect this damage and release cytochrome c into the cytosol. Cytochrome c binds with cytosolic proteins to form an apoptosome, which activates caspase enzymes, initiating apoptosis. |
| death receptor pathway | the pathway of apoptosis which is initiated by the reception of extracellular death signalling molecules. Also known as the extrinsic pathway |
| Death receptor pathway (extrinsic pathway) process | Death signalling molecules can be recognised by death receptor proteins on the surface of cells, and are often released by immune cells. When these molecules bind to a death receptor surface protein, caspase enzymes are activated, initiating apoptosis. |
| what do teh two processes have in common | Following caspase activation, the two pathways become nearly identical. |
| further 4 stage process of apoptosis | 1. Activation of caspases 2. Digestion of cell contents 3. Cell shrinks 4. Membrane blebbing and breakage |
| 1. Activation of caspases | activated by the intrinsic or extrinsic pathway |
| 2. Digestion of cell contents | caspases cleave intracellular proteins, which leads to the breakdown of organelles. |
| 3. Cell shrinks | the cell and nucleus shrink as intracellular material is broken down. |
| 4. Membrane blebbing and breakage | as the cytoskeleton is digested, the cell is weakened. The membrane warps and detaches from the cell in membrane-enclosed vesicles known as apoptotic bodies which contain the broken down intracellular material. |
| what happens after apoptosis | phagocytes engulf and digest the free-floating apoptotic bodies by phagocytosis. |
| phagocytosis | endocytosis of solid material or food particles |
| phagocytes | a cell of the immune system responsible for engulfing and destroying harmful microorganisms and foreign materia |
| when the rate of apoptosis decreases | cell growth can increase exponentially, resulting in the formation of tumours. Tumours can be classified into two categories: • benign tumours and malignant tumours (considered to be cancerous due to their ability to migrate) |
| stem cell | undifferentiated cells with the capability of differentiating into specialised cells |
| process of cells in our body | each cell begins as a stem cell and through the process of differentiation, they develop into specialised cells with a particular function |
| The two properties of stem cells | Self-renewal and potency |
| Self-renewal | Stem cells have the capacity to replicate without disrupting their ability to differentiate by producing both a differentiated cell and a copy of themselves when they replicate |
| potency | Stem cells are undifferentiated cells which can give rise to differentiated cells with a specialised function |
| stem cells equality | not stem cell are equal with some able to differentiate into any cell type, and others capable of differentiating into only a handful of cell types. Based on these relative capabilities, we can categorise stem cells according to their relative potency. |
| Totipotent | Stem cells that can differentiate into any cell type. eg The zygote ( replicates into any cells required to build a foetus) |
| Pluripotent | Stem cells that can differentiate into multiple cell types. eg empryonic stem cells (differentiates into 3 germ layers mesoderm, ectoderm, endoderm) |
| Multipotent | Stem cells that can differentiate into a limited number of specialised cell types belonging to a specific tissue or organ eg bone marrow stem cell which can diffenrtiate into red and white blood cells |
| diagram of potency | zygote (totipotent) differntaites into an embryonic stem cell (pluripotent) which can differntaite into an ectoderm, mesoderm and endoderm (multipotent) an endoderm differentiates into specialised cells like stomach, pancreatic and liver cells. |
| multipotnet cells | ectoderm= neuron, skin cells and pigment cells mesoderm=skeletal muscle,smooth muscle,cardiac muscle, red blood cells and bone cells endoderm=stomach, liver and pancreatic cells |
| NECROSIS | Another way cells die, unregulated death of cells initiated by significant damage which causes the cell to swell, burst, and release cell contents into the surrounding environment. This may lead to inflammation and damage in nearby cells and tissues. |
| when does apoptosis rates decrease | failure to initiate apoptosis not always due to checkpoints,cells may no longer express functional death receptor proteins, leads to death signalling molecules not initiating apoptosis By failing to initiate, cells have a reduced rate of apoptosis. |
| cancer | a disease caused by the uncontrolled replication of cells with the ability to migrate to other parts of the body (only malignant tumours are cancerous as they can migrate) |
| characteristics of cancer cells | Tissue invasion and metastasis |
| what is Tissue invasion and metastasis | When benign tumour cells become malignant/cancerous they are capable of invading nearby layers of tissue and migrating to other parts of the body away from the primary tumour site, typically via the bloodstream or lymphatic system (metastasis). |
| tissue types for animals | Animal bodies are composed of four primary tissue types: Epithelial (covers and protects), Connective (supports and binds), Muscle (enables movement), and Nervous (controls and communicates) |