Interphase
Mitosis
cytokinesis
2 part of cell divison:
growth and repair
reproduction bring babies babies= of spring
reproduction cell divison types: mitosis and meiosis
mitosis is the division of the nucleus of the cell and its content (identical cells)
46 chromosomes in all body cells
they have 2 chromatics 1 centromere( the middle) and they are sister chromatids
sister chromatids are chromatids that form the same chromosome
the longest time in the cell spent in the preparation of cell division = interphase
the cell spends 95% of its time in interphase
there are 3 phases in interphase
G1 2.S 3. G2
the cell cycle = life cycle of the cell
G0 phase is no cell division
extra growth
organelles replication
S = synthesis
DNA replication
it starts with a mother cell the divides into 2 new doughter cells with 46 chromosomes each equaling 92 chromosomes in both
a mother cell is a cell that is going to divide into 2 creating 2 daughter cells
douplicated = 2 chromatids
unduplicated = single
appers only if the cell divide
preparation for cell division
the only cells that dont undergo mitosis are the nerve cell (brain)
the spindle fibers are used to push the chromosome to the middle of the cell
PMAT
prophase
metaphase
anaphase
telophase
nuclear membrane brake apart
chromosomes shorten and condense
centrioles move to opposite pole
centrioles move to opposite poles
sister chromatids line up in the middle of the cell = cell equator
sister chromatids pulled by the spindle fibers to opposite pole
each chromatid now is a seperated chromosome.
nuclear membrame reform
2 new nuclei are formed
chromosome un coiled.
the physical process of separating the cells
animal cell: cleavage furrow is the line between the separating animal cells
plant cells: cells plate is the line between the separating plant cells
living : have cell
cell: basic unit of life
living thing: organism
oranisims have 1 or more cell
ex: bacteria : 1 cell like plants, animals, humans.
all cells have four things which are : cell membrane cytoplasm DNA and organelles
organelles: tiny organ
DNA is in 1.genetics 2. crops 3. diseases
DNAs full name is deoxyribonucleic acid
how many chromosomes do humans have? 46 and 23 pairs
the DNA is located in the nucleus in the chromosome
nucleus: central part of the cell inside chromosomes
the center of a chromosome is called the centromere and thats where 2 chromatids are linked and half of the cromosome is called a chromatid
the dna is up to 2 meters long
gene : its a segment of dna
female is xx male is xy
the shape of the DNA is called a double helix
the genetic code is to build up protein there are 42 protien and 22 cells build up protien
each chromosome is a very long molecule of tightly coild DNA
gene can be used for skin color eye shape and more like that
all genes that form a person is called genome all genes that make ip an organism
DNA: 1. sugar ribose 2.phosphate group 3. nitrogen base
the 4 bases are adenine and thymine and cytosine and guanine
the ones that pair together are adenine and thymine with 2 dots then cytosine and guanine with 3 dots connecting them
the dots represent the hydrogen bond that connects them together
meisosis called reduction divison: reduce the number of chromosomes into half
8 ———> 4 4 4 4
meisis only for sexual reproduction
meiosis makes 4 haploid sex cells which are egg cells (female) and sperm cell (male)
cells that undergo meiosis are called “germ line cells” ←——— sex organs
body cells are: somatic cells → mitosis
there are 46 chromosmes in one cells 44 are autosomes and 2 are sex chromosomes xx for female xy for male
these are types of body cells ( somtic)
skin cell
liver cell
hair cell
autosome: all chromosomes in the cell except sex chromosomes
meiosis division
stages:
prophase 1 ( the longest important stage)
metaphase 1
anaphase 1
telophase 1
prophase 1
→ the crossing over takes place in this stage
→ prophase 1 meiosis 1 is the longest stage of the cell division 90%
→ crossing over takes place betweeen unsister chromatids in the homologous chromosomes
→ crossing over leads to the genetic variation
homologous chromosomes
chromosomes found in pairs each inherited from 1 parent
sister chromatids = chromatids of the same chromosome
tetrad = 4 chromatids
gametes
sperm cells from males egg cell from femal 23 chromosomes come from each to create a gamete
dad has xy chromosomes which decides the gender of the kid while mom has xy
they have 44 autosomes and 2 sex chromosomes which decides the gender
zygote is the joining of sperm and egg
example: ahmed has 44 autosomes and 2 sex chromosomes which are xy showing that hes a male
reproduction
the process of cell division of all living organism to produce offspring = baby
asexual: one parent, identical daughter cells (mitosis)
sexual: male and female (meiosis)
types of cells
somatic = body
have full number of chromosomes = diploid 2n
divide by mitosis
gametes = sex cells
have half number of chromosomes = haploid n
result of meiosis
gametes = sex cells
sperm (male) and egg (female) 23 chromsomes from each
fertilization
the fusion of sprem and egg cell: zygote (2n) diploid
fertilization: the fusion of gametes
zygote
fertilized egg (diploid) = 46 chromsomes
no of chromsomes in 1 somatic cell = 46 chromsomes =23 pairs
22 pair autosomes 1 pair sex chromsomes xx → female xy → male
Trisomy 18 (Edwards Syndrome): This condition involves an extra copy of chromosome 18. It leads to severe intellectual disability, growth deficiencies, and various physical abnormalities. Many affected infants do not survive past their first year.
Trisomy 13 (Patau Syndrome): This syndrome is caused by an extra chromosome 13 and is characterized by severe intellectual disability and physical abnormalities, including heart defects and cleft lip/palate. Like Edwards syndrome, it has a high mortality rate in infants.
Monosomy X (Turner Syndrome): This condition occurs when one of the X chromosomes is missing or partially missing in females. It results in short stature, delayed puberty, and various medical issues. Turner syndrome does not affect intelligence but can lead to other health complications.
Klinefelter Syndrome (47,XXY): This is caused by an extra X chromosome in males and is associated with symptoms such as reduced testosterone levels, infertility, and developmental delays.
Down Syndrome (Trisomy 21): As previously mentioned, it results from an extra copy of chromosome 21 and leads to a variety of developmental and health issues.
GMOs are organisms whose genetic material has been altered using genetic engineering techniques. This process allows scientists to introduce new traits into organisms that would not naturally occur through traditional breeding methods.
Agriculture: Crops can be modified to enhance yield, increase resistance to pests, diseases, and environmental conditions, or improve nutritional content (e.g., Vitamin A in Golden Rice).
Medicine: GMOs are used to produce insulin, growth hormones, and vaccines.
Research: Models like genetically modified mice help in understanding various diseases and conditions.
Increased Crop Resilience: GMOs can withstand herbicides and resist pests, leading to lower agricultural losses.
Reduced Chemical Use: Lower reliance on chemical pesticides can lead to less environmental impact.
Enhanced Nutritional Content: Some GMOs are designed to have improved nutritional benefits.
Health Risks: There are ongoing debates about the long-term health effects of consuming GMOs.
Environmental Impact: Concerns about biodiversity, potential consequences of gene transfer to non-GMO plants, and the impact on ecosystem balance.
Ethical Issues: Debates on the morality of altering natural organisms and corporate control of food supply.
GMOs are a controversial topic with significant advancements in technology that hold the potential for improved food security and health but also raise important ethical, health, and environmental questions.