Growth, asexual reproduction, tissue repair and maintenance are processes that require the creation of new cells In eukaryotic cells, division of the nucleus to form 2 genetically identical nuclei is called MITOSIS The life of the cell can be considered an ordered sequence of events called the cell cycle M - Mitosis and cytokinesis G1 - Growth phase (cell grows and organelle number increase) S - Synthesis phase (chromosomes are replicated in preparation for the next cell division) G2 - Another growth phase (leading to M phase again) Newly produced cells may: grow and reproduce again differentiate to become specialised cells perform a particular function, age then die R – Point – The R-Point is known as the RESTRICTION POINT. It is the most important of the control points of the cell cycle. It is here that the cell determines whether it will undergo mitosis or not. If it has a mutation or is cancerous it may be terminated or remain dormant. Apoptosis is the programmed death of a cell Some cells live for a lifetime (brain cells) others different times Eg. Skin cells (few weeks), stomach lining (few days) and RBCs (few months) Cancer cells avoid apoptosis and continue growing unchecked During Apoptosis, the programmed cell: signals that it is going to die shrinks digestive enzymes are released breaking the cell up some parts are engulfed by macrophages whilst other organelles can be reused by neighbouring cells Cell death is important as: it protects from ill health by destroying infected cells help divide cells in an ordered manner it helps shape organs and tissues Necrosis is a form of cell death that results from irrepairable injury to the cell 4 Phases of Mitosis 1. PROPHASE 2. METAPHASE 3. ANAPHASE 4. TELOPHASE Mitosis is the process used by cells to make new, genetically identical, cells. This is predominantly used in growth and repair INTERPHASE is a phase in a non-dividing cell where all the chromosomes exist in a single chromatid form. Cells spend the majority of their lives in this form P.M.A.T.I OR I.P.M.A.T PROPHASE chromosomes become shorter and fatter by coiling. Repeated coiling is called supercoiling microtubules grow from the poles of the cell and the centrioles these form a spindle called the MITOTIC SPINDLE METAPHASE spindle microtubules attach to the chromosome centromeres chromosomes are moved to the equator. Each chromatid moves to the opposite pole ANAPHASE the pairs of sister chromatids separate, centromeres split and the microtubules pull them to opposite poles TELOPHASE chromatids at each pole gather together and become enclosed in a nuclear membrane the whole cell splits at the equator and forms 2 new cells each cell has the SAME number of chromosomes as the parent cell and contains the same genetic information cell enters INTERPHASE again UNDERSTAND THE PROCESS DON’T MEMORISE THE STEPS VIDEO: CRASHCOURSE MITOSIS VIDEO: THE EUKARYOTIC CELL CYCLE Meiosis is a type of cell division that produces gametes (sex cells) Cells produced are haploid (contain HALF the original chromosome number) Process accounts for great genetic variation due to RANDOM ASSORTMENT CROSSING OVER 2 cell divisions: 1st: PROPHASE I METAPHASE I ANAPHASE I 2nd: PROPHASE II METAPHASE II ANAPHASE II TELOPHASE I TELOPHASE II PROPHASE I cell has 2n (diploid) number of chromosomes chromosomes become visible homologous pairs line-up crossing over occurs and exchange of genetic material (see right) METAPHASE I spindle microtubules move homologous pairs to the equator of the cell orientation of paternal and maternal chromosomes at either side of the equator is random (RANDOM ASSORTMENT) ANAPHASE I Homologous pairs are separated. One chromosome of each pair moves to each pole TELOPHASE I Nuclear membranes form around chromosomes cell membranes form around each nucleus reduction of chromosome number from diploid to haploid is completed (2 haploid cells now formed) cytokinesis occurs PROPHASE II nuclear envelope begins to disintegrate spindle microtubules form chromosomes (with 2 chromatids) condense and become visible METAPHASE II chromosomes line up along the equator (in a straight line) ANAPHASE II centromeres separate and chromatids are moved to opposite poles TELOPHASE II chromatids reach opposite poles nuclear envelope forms cell membrane re-forms cytokinesis occurs At this stage there are 4 GENETICALLY DIFFERENT daughter cells They contain HALF the original chromosome number (haploid) Phase II is very similar to mitosis Random Assortment and Crossing Over play an important role in increasing genetic variation within a species. They do this by increasing the number of different combinations that can be formed in the gametes. CROSSING OVER cont….. During crossing over the 4 chromatids are lined up perfectly next to one another so that the corresponding genes are side by side This process is known as SYNAPSIS and is a bit like doing up a zipper The chromatids are broken at corresponding places and rejoined to form new chromatids. When the chromatids are crossed over the arrangement is called CHIASMATA The inheritance of TOO MANY of TOO FEW chromosomes Not whole chromosome sets, rather INDIVIDUAL CHROMOSOMES The most common aneuploidies are TRISOMIES Eg. Trisomy 21 (Down’s Syndrome) 3 copies of chromosome 21 rather than 2 Aneuploidy can occur in autosomes/sex chromosomes different aneuploidy result in particular chromosome abnormality the older the mother the more likely the occurrence Egs: Trisomy 21 – 3 @ 21 (Down’s Syndrome) Trisomy 13 – 3 @ 13 (Patau Syndrome) 45 - XO (Turner’s Syndrome) 47 - XXX (Klinefelter’s Sydrome) Can result from NON-DISJUNCTION of homologous chromosomes during meiosis The inheritance of additional FULL SETS OF CHROMOSOMES Common in plants – often larger with bigger fruits, flowers and seeds During Anaphase I, if the homologous pair fails to separate then one cell will receive BOTH chromosomes In the 2nd division the paired chromatids separate but the gametes will receive 2 copies of the chromosome Can also result from FAILURE OF PAIRED CHROMOSOMES TO SEPARATE at anaphase II. One gamete receives both chromosomes and the other none VIDEO: CRASHCOURSE MEIOSIS VIDEO: NON-DISJUNCTION VIDEO: CROSSING OVER AND GENETIC VARIABILITY