cellstructure& genetic control

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Cell Structure and Genetic Control www.freelivedoctor.com

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Page 1: Cellstructure& Genetic Control

Cell Structure and Genetic Control

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Page 2: Cellstructure& Genetic Control

Cell

Basic unit of structure and function of the body. Highly organized molecular factory.

Great diversity of function. Organ physiology derived from complex

functions of the cell. 3 principal parts:

Plasma membrane. Cytoplasm and organelles. Nucleus.

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Page 3: Cellstructure& Genetic Control

Plasma Membrane

Is selectively permeable. Composition:

Double layer of phospholipids due to hydrophobic/hydrophilic parts.

Restrict passage of H20 and H20 soluble ions. Proteins span or partially span the membrane.

Provide structural support, transport molecules, serve as receptors.

Negatively charged carbohydrates attach to the outer surface.

Involved with regulatory molecules.

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Page 4: Cellstructure& Genetic Control

Plasma Membrane (continued)

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Page 5: Cellstructure& Genetic Control

Cytoplasm, Organelles, Nucleoli

Cytoplasm: Aqueous content of the cell.

Organelles: Sub-cellular structures within the cytoplasm.

Nucleus: Is a large spheroid body. Largest of the organelles. Contains the genetic material (DNA). Nucleoli:

Centers for production of ribosomes.

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Page 6: Cellstructure& Genetic Control

Cytoplasm, Organelles, Nucleoli (continued)

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Page 7: Cellstructure& Genetic Control

Bulk Transport

Phagocytosis: Phagocytic cells use pseudopods to surround and engulf

particles. Pseudopods join, fuse, and surround ingested particle (food

vacuole). Lysosomes digest food vacuole.

Protects from invading organisms. Removes debris.

Endocytosis: Pinocytosis:

Nonspecific process. Plasma membrane invaginates, fuses, vesicle containing ECF

pinches off, and vesicle enters cell.

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Page 8: Cellstructure& Genetic Control

Bulk Transport (continued)

Receptor-mediated endocytosis: Interaction of molecules in ECF with specific membrane

receptor proteins. Membrane invaginates, fuses, pinches off and forms

vesicle. Vesicle enters cell.

Exocytosis: Process by which cellular products are secreted into

extracellular environment. Proteins and other molecules to be secreted are packaged

in vesicles by Golgi complex. Vesicles fuse with plasma membrane and release contents

into extracellular environment.

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Page 9: Cellstructure& Genetic Control

Cilia, Flagella, Microvilli

Cilia: Tiny hair-like structures that project from

the surface of the cell. Stroke in unison.

Respiratory tract, uterine tube.

Flagella: Simple whip-like structure that propels

sperm through its environment. Microvilli:

Numerous folds (finger-like projections) increase surface area.

Aid absorption.www.freelivedoctor.com

Page 10: Cellstructure& Genetic Control

Cytoplasm and Cytoskeleton

Cytoplasm: Jelly-like matrix within

the cell. Includes organelles

and cytosol. Highly organized

structure with microtubules and microfilaments that function as cytoskeleton.

Cytoskeleton: Actin and myosin

(microfilaments). Spindle apparatus

(microtubules). www.freelivedoctor.com

Page 11: Cellstructure& Genetic Control

Lysosomes

Primary: Contain only digestive enzymes.

Secondary: Primary lysosome fuses with food vacuole or

organelle. Contain partially digested remnants of other organelles

and organic material. Residual body:

Contain undigested wastes. Autophagy:

Process that destroys worn-out organelles, so that they can be continuously replaced.

Apoptosis (programmed cell death): Lysosomes release digestive enzymes into the cell.

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Page 12: Cellstructure& Genetic Control

Peroxisomes

Membrane-enclosed organelles. Contain specific enzymes that promote

oxidative reactions. Oxidize molecules and form H202.

Catalase: converts H202 H20 + 02.

Oxidation of toxic molecules by peroxisomes is an important function of liver and kidney cells.

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Page 13: Cellstructure& Genetic Control

Mitochondria

Sites for energy production of all cells; but mature RBCs.

Contain own DNA, can reproduce themselves.

Structure: Outer membrane:

smooth. Inner membrane: cristae. Cristae and matrix

compartmentalize mitochondrion space.

Have different roles in energy generation.

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Page 14: Cellstructure& Genetic Control

Ribosomes

Protein factories: Proteins produced according to genetic

information contained in mRNA. Located in cytoplasm and on the surface of

endoplasmic reticulum. rRNA molecules serve as enzymes

(ribozymes) required for protein synthesis. Contains 2 subunits composed of rRNA and

proteins.

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Page 15: Cellstructure& Genetic Control

Endoplasmic Reticulum (ER)

Granular (rough) ER: Bears ribosomes on

surface, in cells active in protein synthesis.

Proteins enter cisternae are modified for secretion.

Agranular (smooth) ER:

Provides site for enzyme reactions in steroid hormone production and inactivation.

Storage of Ca2+ in striated muscle cells.

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Page 16: Cellstructure& Genetic Control

Golgi Complex

Stacks of hollow, flattened sacks with cisternae.

One side of sack faces site for entry of vesicles from ER that contain cellular products.

Other site faces towards plasma membrane and releases vesicles of chemically modified products.

Modifies proteins, separates according to destination, and packages into vesicles.

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Page 17: Cellstructure& Genetic Control

Cell Nucleus

Most cells have single nucleus. Enclosed by inner and outer membrane

(nuclear envelope). Outer membrane is continuous with ER.

Nuclear pore complexes fuse inner and outer membranes together. Selective active transport of proteins and RNA.

Regulation of gene expression. Transport of mRNA out of nucleus to ribosomes.

Nucleoli: DNA contains the genes that code for the

production of mRNA.

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Page 18: Cellstructure& Genetic Control

Chromatin

DNA within nucleus combines with protein (histones) to form chromatin.

Thread-like material that makes up the chromosomes. Histone proteins are positively charged and form spools

around which the negatively charged DNA strands wrap. Euchromatin:

Active in genetic transcription. Heterochromatin:

Contains genes that are permanently inactivated.

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Page 19: Cellstructure& Genetic Control

Chromatin (continued)

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Page 20: Cellstructure& Genetic Control

RNA Synthesis

One gene codes for one polypeptide chain. Each gene is several thousand nucleotide

pairs long (DNA). Each gene contains the code for the

production of a particular type of mRNA. For the genetic code to be translated into

synthesis of a particular protein, the DNA code is copied onto a strand of RNA (genetic transcription).

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Page 21: Cellstructure& Genetic Control

Genetic Transcription

RNA-polymerase breaks weak hydrogen bonds between paired bases of DNA.

Regulatory molecules act as transcription factors by binding to promoter region of gene, activating the gene.

Double stranded DNA separates at region to be translated.

One freed strand of DNA serves as guide.

Freed bases pair with complementary RNA nucleotide bases.

RNA detaches.www.freelivedoctor.com

Page 22: Cellstructure& Genetic Control

Types of RNA

4 types of RNA produced within nucleus by transcription. Precursor mRNA pre-mRNA):

Altered in nucleus to form mRNA. Messenger RNA (mRNA):

Contains the code for synthesis of specific proteins.

Transfer RNA (tRNA): Decodes genetic message contained in mRNA.

Ribosomal RNA (rRNA): Forms part of the ribosome structure.

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Page 23: Cellstructure& Genetic Control

Pre-mRNA

Contains excess bases within the pre-mRNA.

Introns: Regions of non-coding

DNA within a gene. Exons:

Coding regions. Introns are removed

and the ends of exons spliced by snRNPs to produce mRNA.

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Page 24: Cellstructure& Genetic Control

Protein Synthesis

Each mRNA passes through ribosomes forming a polyribosome.

Association of mRNA with ribosomes is needed for genetic translation.

Translation: Production of specific protein according to

code contained in mRNA base sequence.

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Protein Synthesis (continued)

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Page 26: Cellstructure& Genetic Control

Protein Synthesis (continued)

Each mRNA contains hundreds of nucleotides arranged in sequence determined by the complementary base pairing with DNA.

Codon: Each 3 bases (triplet) is a code word for a

specific amino acid.

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Page 27: Cellstructure& Genetic Control

Protein Synthesis (continued)

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Page 28: Cellstructure& Genetic Control

Transfer RNA

Translation of the codons accomplished by tRNA and enzymes.

tRNA bends on itself, making an anticodon (3 nucleotides that are complementary to codon of mRNA).

Synthetase enzymes join specific amino acids to the ends of tRNA within a given codon.

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Page 29: Cellstructure& Genetic Control

Formation of a Polypeptide

Anticodons of tRNA binds to mRNA codons.

Each tRNA carries a specific amino acid. tRNA bring amino acids close together. Amino acid detaches from tRNA.

Enzymatically this amino acid is transferred to the amino acid on the next tRNA.

Polypeptide chain grows. Interactions between amino acids cause

chain to twist and fold forming secondary and tertiary structure.

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Page 30: Cellstructure& Genetic Control

Translation of mRNA

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Page 31: Cellstructure& Genetic Control

Functions of ER and Golgi Complex

Proteins to be secreted by the cell are synthesized by mRNA-ribosome complexes located on granular ER. Proteins enter the cisternae, and are

modified. Leader sequence of amino acids is

attracted to membranes of ER. Once proteins are in cisternae, the leader

sequence is removed. Enzymatic removal of regions in protein, alter

structure.

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Page 32: Cellstructure& Genetic Control

Functions of ER and Golgi Complex (continued)

Secretory proteins are transported to Golgi complex. Further modified, packaged in vesicles, and secreted.

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Page 33: Cellstructure& Genetic Control

DNA Replication

DNA is the only molecule in the body capable of replication.

DNA helicases break weak hydrogen bonds to produce 2 free strands of DNA.

Bases of each of the freed DNA strands can bind to complementary bases.

Each copy is composed of one new strand and one strand from the original DNA molecule.

Preserves the sequence of bases in DNA.

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Page 34: Cellstructure& Genetic Control

DNA Replication (continued)

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Page 35: Cellstructure& Genetic Control

DNA

Law of Complementary Base Pairings: # of purine bases = # pyrimadine

bases. Adenine only pairs with thymine. Guanine only pairs with cytosine. DNA polymerases join the nucleotides

together to form a second polynucleotide chain.

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Page 36: Cellstructure& Genetic Control

Cell Cycle

Interphase (non-dividing cell phases): G1:

Produces mRNA and proteins. S:

If cell is going to divide, DNA replicated. G2:

Chromosome consists of 2 chromatids joined by centromere.

Each chromatid contains a complete double-helix DNA molecule. Each chromatid will become a separate chromosome once mitotic division completed.

Completes interphase.

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Page 37: Cellstructure& Genetic Control

Cyclins

Cyclins promote different phases of the cell cycle. During G1 phase an increase in cyclin D proteins activates

enzymes to move the cell quickly through the G1 phase. Overactivity of a gene that codes for cyclin D might cause

uncontrolled cell division (cancer). Oncogenes:

Mutated forms of normal genes that contribute to cancer. Tumor suppressor genes:

Inhibit cancer development. Suppressor gene p53 indirectly blocks the ability of cyclins

to stimulate cell division. Induces the expression of gene p21, which inactivates the

cyclin-dependent kinases. Promotes cell differentiation.

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Page 38: Cellstructure& Genetic Control

Mitosis (M Phase)

Prophase: Chromosomes become visible distinct structures.

Metaphase: Chromosomes line up single file along equator.

Action of spindle fibers attached to kinetochore Anaphase:

Centromeres split apart. Spindle fibers shorten, pulling the 2 chromatids in

each chromosome to opposite poles. Telophase:

Division of cytoplasm, producing 2 daughter cells.

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Page 39: Cellstructure& Genetic Control

Mitosis (continued)

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Page 40: Cellstructure& Genetic Control

Mitosis (continued)

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Page 41: Cellstructure& Genetic Control

Role of Centrosome

All animal cells have centrosome, located near nucleus in non-dividing cell.

At center are 2 centrioles. Each centriole composed of 9 bundles of microtubules.

Microtubules grow out of pericentriolar material. Centrosome replicates itself during interphase (if cell is

going to divide). Identical centrosomes move away from each other

during prophase. Take up opposite poles by metaphase.

Microtubules from both centrosomes form spindle fibers. Spindle fibers pull chromosomes to opposite poles during

anaphase.

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Page 42: Cellstructure& Genetic Control

Telomeres and Cell Division

Decreased ability of cells to divide is an indicator of senescence (aging).

May be related to the loss of DNA sequences at the ends of chromosomes (regions called telomeres).

Telomeres serve as caps on the ends of DNA. Prevent enzymes from mistaking the normal ends for broken

DNA. DNA polymerase does not fully copy the DNA at end-regions.

Each time a chromosome replicates it loses 50-100 base pairs in its telomeres.

Germinal cells can divide indefinitely due to an enzyme telomerase.

Duplicates telomere DNA.

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Page 43: Cellstructure& Genetic Control

Meiosis (Reduction Division)

Cell division occurring in ovaries and testes to produce gametes (ova and sperm cells).

Has 2 divisional sequences: First division:

Homologous chromosomes line up side by side along equator of cell.

Spindle fibers pull 1 member of the homologous pair to each pole.

Each of the daughter cells contains 23 different chromosomes, consisting of 2 chromatids.

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Page 44: Cellstructure& Genetic Control

Meiosis (Reduction Division)

(continued)

Second division: Each daughter cell divides, with duplicate

chromatids going to each new daughter cell. Testes: produce 4 sperm cells. Ovaries: produce one mature egg, polar bodies

die.

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Page 45: Cellstructure& Genetic Control

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Page 46: Cellstructure& Genetic Control

Cell Death

Pathologically: Cells deprived of blood supply swell, the membrane

ruptures, and the cell bursts (necrosis). Apoptosis:

Cells shrink, membranes become bubbled, nuclei condense.

Capsases (“executioner enzymes”): Mitochondria membranes become permeable to

proteins and other products. Programmed cell death:

Physiological process responsible for remodeling of tissues during embryonic development and tissue turnover in the adult.

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