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Chapter 17 From Gene to Protein.

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Presentation on theme: "Chapter 17 From Gene to Protein."— Presentation transcript:

1 Chapter 17 From Gene to Protein

2 Central Dogma of Molecular Biology
DNA RNA Protein

3 Metabolic control Gene to protein relationship 1st proposed by
Garrod: inherited diseases reflect inability to make a particular enzyme “inborn errors of metabolism”

4 Beadle & Tatum’s experiment
Studying Neurospora (fungus) supported “one gene – one enzyme” & modified to “one gene – one polypeptide” Nucleic acids & proteins are informational polymers assembled from linear sequences of nucleotides & amino acids, respectively

5 Figure 17.1 Beadle and Tatum’s evidence for the one gene-one enzyme hypothesis

6 Figure 17.2 Overview: the roles of transcription and translation in the flow of genetic information

7 Figure 17.3 The triplet code

8 Transcription (mRNA synthesis)
Catalyzed by RNA polymerase (Initiation, Elongation, Termination) DNA portion (one gene in length) unwinds, unzips Free RNA nucleotides pair up on 1 of the DNA strands Promoters signal initiation of transcription until terminator sequence is reached, then it breaks off & DNA rejoins & rewinds Modified, then mRNA travels to cytoplasm

9 Figure 17.6 The stages of transcription: initiation, elongation, and termination (Layer 1)

10 Figure 17.6 The stages of transcription: initiation, elongation, and termination

11 Figure 17.6 The stages of transcription: initiation, elongation, and termination

12 Figure 17.6 The stages of transcription: initiation, elongation, and termination (Layer 4)

13 Figure 17.6 The stages of transcription: elongation

14 Figure 17.7 The initiation of transcription at a eukaryotic promoter

15 Translation (Protein synthesis)
(Initiation, Elongation, Termination) tRNA’s pick up specific AA’s based on anticodon & carry AA’s to mRNA attached to a ribosome ATP driven process catalyzed by many AA activating enzymes P and A sites of ribosome help hold mRNA & tRNA together; peptide bond forms, mRNA moves down the ribosome (made of protein & rRNA)

16 Figure 17.12 Translation: the basic concept

17 Figure 17.13a The structure of transfer RNA (tRNA)

18 Figure 17.13b The structure of transfer RNA (tRNA)

19 Figure 17.15 The anatomy of a functioning ribosome

20 Figure 17.17 The initiation of translation

21 Translation mRNA is freed from ribosome & AA chain
Proteins functioning on membranes or exported from cell are synthesized on ribosomes on rough ER

22 Figure 17.18 The elongation cycle of translation

23 Figure 17.19 The termination of translation

24 Figure Polyribosomes

25 Figure 17.21 The signal mechanism for targeting proteins to the ER

26 Figure 17.22 Coupled transcription and translation in bacteria

27 The Genetic Code Determined in early 1960’s
codon – 3-base unit (triplet) that codes for 1 AA anticodon – 3-base unit on tRNA which is complementary to codon on mRNA All codons don’t code for AA (43 codons) Most genes are interrupted by introns – long noncoding regions

28 Figure 17.4 The dictionary of the genetic code

29 Eukaryotic RNA processing
Removing (excising) introns & joining exons by RNA splicing triggered by sets of nucleotides at either end of intron Splicing catalyzed by small nuclear ribonucleoproteins (snRNP’s) consisting of small nuclear RNA (snRNA) & proteins operating within larger groups called spliceosomes

30 Figure 17.8 RNA processing; addition of the 5 cap and poly(A) tail

31 Figure 17.9 RNA processing: RNA splicing

32 Figure 17.10 The roles of snRNPs and spliceosomes in mRNA splicing

33 Eukaryotic RNA processing
Eukaryotic mRNA receives a modified GTP cap at the 5’ end and a poly-A tail (stretch of nucleotides) at the 3’ end (protects from degradation & enhance translation) 30 – 200 adenine nucleotides (poly–A)

34 Figure 17.11 Correspondence between exons and protein domains

35 Mutations 1) base pair substitutions - point mutations
2) base pair insertions/deletions - frameshift 3) conditional mutations – harmful under certain environmental conditions (high/low temp. if temp. sensitive) 4) spontaneous mutations – may occur during replication or repair

36 Figure 17.23 The molecular basis of sickle-cell disease: a point mutation

37 Figure 17.24 Categories and consequences of point mutations: Base-pair substitution

38 Figure 17.24 Categories and consequences of point mutations: Base-pair insertion or deletion

39 Figure 17.25 A summary of transcription and translation in a eukaryotic cell


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