1. Chapter 13 Regulation of Gene Expression

2. Section 1 Principles and Concepts

3. § 1.1 Concepts Gene: A DNA segment that contains the all genetic information required to encodes RNA and protein molecules. Genome: A complete set of genes of a given species. Gene expression: A process of gene transcription and translation.

4. Specificity of gene expression Temporal specificity (also called stage specificity): why in the infant not in the aged ones? Spatial specificity (also called tissue specificity): why in liver not in brain?

5. Specificity of gene expression

6. Type of gene expression a. Constitutive expression Some genes are essential and necessary for life, and therefore are continuously expressed, such as those enzymes involved in TAC. These genes are called housekeeping genes.

7. b. Induction and repression The expression levels of some genes fluctuate in response to the external signals.

8. Some genes demonstrate higher expression level once being activated. It is called induced expression. On the other hand, some genes are repressed and their expression levels are lower. It is called repressed expression.

9. § 1.2 Regulatory Elements Gene expression is a multiple-level process. Transcription initiation is a key point of controlling gene expression.

10. Basic elements that regulate the transcription include: a.Special DNA sequences b.Regulatory proteins c.DNA-protein interaction and protein-protein interaction d.RNA polymerase

11. For prokaryotic systems: Operon is composed of structural genes, promoter, operator, and other regulatory sequences. a. Special DNA sequence Other requlatory sequence Operator Promoter Sturctural genes

12. The DNA sequence that RNA-pol can bind to and initiate the transcription. Promoter

13. The DNA sequence adjacent to the structural genes that the repressor protein can bind to and prevent the transcription of structural genes. Operator

14. Cis-acting elements is the special DNA sequence that can affect the expression of its own gene. For eukaryotic systems:

15. b. Regulatory proteins For prokaryotic systems: Specific factor: It facilitates the binding of RNA-pol to particular DNA sequence. Repressor: It binds to the operator and prevent the transcription, known as negative regulation.

16. Activator: It associates with DNA near the initiation point, resulting in the increase of RNA-pol binding affinity and the enhancement of the transcription efficiency.

17. For eukaryotic systems: The regulatory proteins are called transcription factors (TF). After expression, TF will interact with the cis-acting elements to activate another genes. Therefore, they are referred to as trans-acting factors.

18. Trans-acting factors

19. The regulation is implemented through numerous interactions between cis-acting elements and trans-acting factors. They are non-covalent bond. c. DNA-protein interactions

20. Proteins may have to interact with each other prior to the DNA binding. Proteins can form a homo or hetero- dimer form to function properly. Present in prokaryotes as well as eukaryotes. Protein-protein interactions

21. Section 2 Gene Regulation of Prokaryotic Systems

22. Common features Prokaryotic genes are polycistron systems, that is, several relevant genes are organized together to form a transcription unit --- operon. The majority of gene regulation is negative. Inducers are used to remove the repression.

23. Operon is a coordinate unit for the regulation. Transcription initiation is the key point for regulation. Translation can also be regulated. §2.1 Regulation of Transcription

24. Structure of lac operon

25. Metabolism of lactose

26. Bacteria do not express these three enzymes when glucose is available. However, bacteria produce those enzymes if lactose is present and glucose is absent. Inducible expression

27. Sequence of lac operon lac operon (TTTACA/TATGTT) is a weak promoter, and has a basal expression level. CAP (Catabolite gene activator protein) binding site is at -60 region. CAP is a homodimer with binding ability to DNA and cAMP.

28. Glucose inhibits the formation of cAMP. When glucose is present, [cAMP] is lower. Only after glucose is exhausted, [cAMP] becomes higher. The CAP-cAMP complex is formed, and this complex binds to the CAP binding site on lac operon.

29. When lactose is absent, no lac gene is expressed. Situation 1

30. lacI gene has its own promoter, and its expression can produce LacI repressor. The tetrameric Lac repressor binds to the lac operator site O lac. The binding blocks the RNA-pol moving on DNA template, and no lacZ, lacY, and lacA are expressed.

31. galactosidase Situation 2 When lactose is present, lacZ, lacY, and lacA genes are expressed.

32. The galactosidase is weakly expressed (at the basal level). When lactose is present, it is converted to allolactose or galactose that binds to the repressor. The repressor can no longer bind to the operator, and lac gene can be expressed. Galactose, Allolastose and IPTG are referred to as inducer.

33. Inducers

34. The lacZYA RNA transcript is very unstable and could be degraded quickly. Therefore, the synthesis of three enzymes will be cease under normal condition. Presence of lactose

35. When glucose is present, the [cAMP] is low, no CAP-cAMP is formed and the expression of the lac operon is still low. Situation 3

36. When glucose is absent and lactose is present, the CAP-cAMP complex binds to the CAP site to activate the lac gene. Situation 4

37. Coordinate expression No glucose Glucose

38. §2.2 Transcription Attenuation The trp operon is one of the constitutive genes expressed at the basal level. The structural gene of trp operon encodes 5 enzymes used for the synthesis of Trp. Trp operon

39. The trp repressor gene can be expressed, but it does not bind to the operator. When Trp is more than enough, the repressor will form a complex with Trp. The complex binds to the operator, blocking the synthesis of Trp.

40. Trp operon

41. Attenuation mechanism In addition to the repressor regulation, trp gene has a fine tuning mechanism called attenuation. The trp operon is regulated using attenuation mechanism at the translation level.

42. Leader sequence

43. Possible hairpins 1/2 and 3/4 hairpin structure 2/3 hairpin structure

44. High Trp concentration

45. Low Trp concentration

46. Under the normal conditions, the LexA gene expressed to repressor proteins that bind to promoters of other genes and block their expressions. Once the repressors are degraded, the repressed genes will be expressed. At the basal level, the normal cell contains about 1000 copies of RecA protein. §2.3 Protein Degradation

47. SOS response

48. LexA digestion

49. When DNA is extensively damaged, DNA replication is halted and the number of ssDNA gaps increases. The RecA protein binds to this damaged ssDNA, which activates the protein’s coprotease activity. While bound to ssDNA, the RecA protein facilitates the cleavage of LexA repressor as well as the inactivation of the LexA repressor.

50. §2.4 Genetic Recombination

51. An RNA, with sequence complementary to a specific RNA transcript or mRNA, whose binding prevents processing of the transcript or translation of the mRNA. Antisense RNA

53. Section 3 Regulation of Eukaryotic Transcription

54. Structural features Large genome: 3 x 10 9 bps, 35 000 genes Monocistron Repeated sequences: different lengths and different frequencies. Often inverted repeats Splite genes: separated by introns and exons alternatively

55. Regulation features 1. RNA-pol: 3 forms (I, II, and III) for different RNAs 2. Changes of chromosomal structure Hypersensitive site Base modification Isomer-conversion Histone changes

56. 3. Positive regulation 4. Transcription and translation are separated 5. Post-transcriptional modification 6. Regulation through intercellular and intracellular signals

57. §3.1 Cis-acting elements They are specific DNA sequences, each of which regulates transcription of one or more genes. They usually have consensus sequences. Promoter: TATA box, CAAT box, and GC box,

58. Sequence: TATAAAA Location: - 25 ~ - 30 bp Function: It is the binding site for TFII D, which is required for RNA polymerase binding. It controls the veracity and frequency of transcriptional initiation. TATA box

59. Sequence: GCCAAT Location: ~ -70 bp Function: It is the binding site for CTF1 (CAAT-binding transcription factor) and C/EBP (enhancer binding protein). CAAT box

60. Sequence: GGGCGG Location: -30 ~ -110 bp Function: It is the binding site for a protein called Sp1. GC box

61. It is a DNA sequence that can determine the temporal and spatial specificities of expression and increase the promoter activity. enhancer

62. It is a negative regulation element. It will repress the transcription once interacted with specific proteins. Silencer

63. §3.2. Trans-acting factors They are the proteins that bind indirectly to cis-acting elements and then regulate the transcription initiation. The trans-acting factors can be transcription factors (TF).

64. transcription factors General transcription factors Special transcription factors –Transcription activators EBP (enhancer binding protein) –Transcription inhibitors

65. General structure of TF DNA-binding domain Activation domain Protein-protein interaction domain

66. Promoter and regulatory proteins

67. General structure of TF CTD of RNA-pol II is an important point of interaction with mediators and other protein complexes. Cofactors facilitate the TF assembly.

68. Transcription repressor

69. §3.3 DNA-protein interactions Regulatory proteins have discrete DNA-binding domains of particular structure, i.e., binding motif. The AA side chains of regulatory proteins interact with bases of DNA through H bonds.

71. Yeast activator protein GCN4 Leucine zipper

74. Zinc finger

75. Steroid hormone receptor

76. Mouse regulatory protein Zif268 Zinc finger

77. Helix-loop-helix

78. Human transcription factor MAX

79. Helix-turn-helix Lac repressor

80. Helix-turn-helix Trp repressor