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Central Dogma Protein Synthesis Two types of nucleic acids # of strands kind of sugar bases used The Importance of Protein Synthesis Specific Roles: • Enzyme action • Transport • Motion • Protection • Support • Communication • Regulation Examples: •Protein antibodies for immune system •Hair, nails, skin •Hemoglobin in blood •Insulin to regulate blood sugar levels Central Dogma DNA is the genetic material within the nucleus. Replication The process of replication creates new copies of DNA. The process of transcription creates an mRNA using DNA information. DNA Transcription RNA Nucleus The process of translation creates a protein using mRNA information. Translation Protein Cytoplasm Protein Synthesis Transcription Translation Transcription • The new RNA molecule is formed by incorporating nucleotides that are complementary to the template strand. DNA coding strand 5’ 3’ DNA G T C A T T C G G 3’ G U C A U U C G G 3’ C A G T A A G C C 5’ DNA template strand 5’ RNA Where to Begin Transcription Production of mRNA copy of the DNA gene Translation •The process of reading the RNA sequence of an mRNA and creating the amino acid sequence of a protein is called translation. DNA template DNA Transcription T T C A G T C A G A A G U C A G U C strand Messenger RNA mRNA Codon Codon Codon Translation Protein Lysine Serine Valine Polypeptide (amino acid sequence) Codon •Translation will always begin with a start codon “AUG” (Start) and end with the “TAG” (end) Translation Termination Stop codon Ribosome reaches stop codon 5’ mRNA A U G G G A U G U A A G C G A U A A P Release factor A Translation Termination Once stop codon is reached, elements disassemble. Release factor P A Who am I? Messenger RNA a.k.a. mRNA Copied from DNA, conveys information from chromosomes to ribosomes. Every three nucleotides is a codon. Who am I? Transfer RNA a.k.a. tRNA Transports amino acids to ribosomes. Who am I? Ribosomal RNA a.k.a. rRNA Subunits where the protein is assembled Translation Synthesis of proteins by ribosomes Genes • Genes: a set of instructions encoded in the DNA sequence of each organism that specify the sequence of amino acids in proteins characteristic of that organism. In eukaryotes, many general are interrupted by introns and exons. • Introns – long segments of nucleotides that have no coding information. • Exons – are the portions of a gene that are translated (expressed) into proteins. Protein Synthesis General Pathway Prokaryotes vs Eukaryotes Protein Synthesis Prokaryotes Eukaryotes •In prokaryotes, mRNA •The initial RNA transcript, in the nucleus, is transcripts of a coding while composed of exons, and sequence are copied introns. from the DNA as a •Before leaving the nucleus, introns are removed and splice single contiguous exons together. sequence. •The processed transcript, then properly called mRNA and carrying the appropriate codon sequence for a protein, is transported from the nucleus to the ribosome for translation. Tay-Sachs • A baby with Tay-Sachs disease appears healthy at birth. Symptoms usually first appear 3 to 6 months after birth, beginning with mild motor weakness and occasional twitches of the eye (myoclonic jerks). By 6 to 10 months of age, the baby's motor skills may be lost. After this, the diseases progresses rapidly to seizures, blindness, paralysis, and death at age 4 to 5. Mutations • Mutations are permanent changes in the sequence of nitrogen-containing bases in DNA. • Mutations occur when base pairs are incorrectly matched (e.g., A bonded to C rather than A bonded to T) and can, but usually do not, improve the product coded by the gene. • Inserting or deleting base pairs in an existing gene can cause a mutation by changing the codon reading frame used by a ribosome. • Mutations that occur in somatic, or nongerm, cells are often not detected because they cannot be passed on to offspring. They may, however, give rise to cancer or other undesirable cellular changes. • Mutations in the germline can produce functionally different proteins that cause such genetic diseases as Tay-Sachs, sickle cell anemia, and Duchenne muscular dystrophy. Duchenne muscular dystrophy • In individuals with the disorder, initial findings may include an unusual, waddling manner of walking (gait); difficulty climbing stairs or rising from a sitting position; and repeated falling. Duchenne muscular dystrophy If it gets worse more problems can occur like • Progressive curvature of the spine • Wasting of thigh muscles and abnormal enlargement of the calves • Abnormal fixation of certain joints (joint contractures) due to muscle weakness • Prolonged immobility • Shortening of muscle fibers • By approximately age 10 to 12, most affected individuals require the use of a wheelchair. Warm-Up • The DNA in each of your cells are exactly alike. How come so many of your cells look completely different? • Now talk to the person sitting next to you and see what they came up with. • What does trans mean? • What does scribe mean? • What would transcribe mean? Structure of DNA •DNA Base Pairing Rules •A T •C G