Viral DNA replication

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Viral DNA replication Lecture 8 Biology 3310/4310 Virology Spring 2017 The more the merrier --ANONYMOUS

Viral DNA genomes must be replicated to make new progeny Parvovirus Retrovirus Poliovirus VII Hepatitis B virus Adenovirus Herpes simplex virus Polyoma- and Papillomaviruses Reovirus Rotavirus Influenza virus

Universal rules of DNA replication Base 5-3 - Primer -3 OH P OH -5 Direction Of Chain Growth DNA is synthesized by template-directed incorporation of dnmps into 3 -OH of DNA chain DNA is always synthesized 5-3 via semiconservative replication (two daughter strands) Replication initiates at specific sites on template called origins Catalyzed by DdDp + accessory proteins Always primer-dependent

Base P 5 - Primer OH -3 OH -5 3 - Direction Of Chain Growth

What s the host for? Viruses can t do it themselves Viral DNA replication always requires synthesis of at least one viral protein, sometimes many (hence always delayed after infection) Simple viruses require more host proteins - genetic economy Complex viruses encode many, but not all proteins required for replication

Where does the polymerase come from? Small DNA viruses do not encode an entire replication system - Encode proteins that orchestrate the host - Papillomaviridae, Polyomaviridae, Parvoviridae Large DNA viruses encode most of their own replication systems - Herpesviridae, Adenoviridae, Poxviridae

Viral proteins DNA polymerase and accessory proteins Origin binding protein, helicases Exonucleases Enzymes of nucleic acid metabolism (thymidine kinase, ribonucleotide reductase, dutpase)

Go to: b.socrative.com/login/student room number: virus Which statement about viral DNA synthesis is NOT correct? A. Large DNA viruses encode many proteins involved in DNA synthesis B. Small DNA viruses encode at least one protein involved in DNA synthesis C. Viral DNA replication is always delayed after infection because it requires the synthesis of at least one viral protein D. Some viruses encode all proteins needed for DNA replication 1

Diverse viral genome structures

Two mechanisms of dsdna synthesis RNA primers Never RNA primed

The 5 -end problem

Lessons from SV40 ~5 kbp

Semi-discontinuous DNA synthesis from a bidirectional origin No end problem!

Recognition and unwinding of SV40 origin Rp-A binds LT! T has 3-5 helicase activity

Synthesis of leading and lagging strands Primase binds Rp-A and LT Synthesis of RNA primers Synthesis of short DNA fragments Rf-C binds 3 OH along with PCNA and pol δ RF-C a clamp loading protein Allows entry of PCNA on DNA Causes release of pol α Form sliding clamps along DNA Synthesis of long DNA

Synthesis of leading and lagging strands

Function of topoisomerases

Go to: b.socrative.com/login/student room number: virus The SV40 genome is a circular dsdna. Which statement about its replication is correct? A. Viral T antigen binds and unwinds the ori B. Replication is bidirectional from a single ori C. The 5 -end problem is solved D. Has leading and lagging strand synthesis E. All of the above 2

DNA priming: Parvoviruses ori

DNA priming: Parvoviruses Replication is continuous No pol α, uses ITR to self-prime Requires pol δ, RF-C and PCNA Rep78/68 proteins are required for initiation and resolution: endonuclease, helicase, binds 5 -terminus No replication fork, strand displacement No end problem!

Protein priming: Adenovirus Origins at both ends Strand displacement synthesis Semiconservative DNA replication

Protein priming: Adenovirus Ad DNA pol links α-phosphoryl of dcmp to OH of Ser residue only when ptp is assembled with DNA pol into preinitiation complex at ori ITRs No end problem!

Adenoviral ssdna binding protein

Go to: b.socrative.com/login/student room number: virus How is DNA replication of parvovirus and adenovirus similar? A. They both require protein-linked primers B. Replication occurs by strand displacement C. DNA synthesis occurs in the cytoplasm D. A replication fork occurs in both E. None of the above 3

Herpes simplex virus UL5, 8 and 53 - primase UL42 - processivity protein UL9 - origin binding protein UL29 - ssdna binding protein UL30 - DNA polymerase 2 oris and a unique oril sequence DNA enters as a linear molecule and converts to circle Replicates as rolling circle

Initiation of herpesvirus DNA replication DNA ligase IV/XRCC4 Host proteins are responsible for circularization

Rolling circle replication No end problem!

Poxvirus All viruses discussed replicate in nucleus Poxviruses replicate in cytoplasm

Poxvirus DNA factories DNA DNA binding protein merge

Poxvirus DNA replication At least 15 viral proteins involved in viral DNA synthesis No end problem!

Go to: b.socrative.com/login/student room number: virus What makes poxvirus DNA replication different from all of the other viruses we discussed today? A. The complete replication machinery is encoded by the viral genome B. DNA synthesis occurs in the nucleus C. DNA synthesis occurs by strand displacement D. None of the above 4

Viral origins Ori AT-rich segments recognized by viral origin recognition proteins Assembly points for multi-protein DNA replication machines Some viral genomes have one ori; others up to 3

Viral origins of DNA replication

Viral origin recognition proteins Polyomavirus T binds specifically to DNA Papillomavirus E1 binds ori in presence of E2 Parvovirus Rep68/78 binds at ends and unwinds DNA, also involved in terminal resolution Adenovirus ptp binds at terminus and recruits DNA pol Herpesvirus UL9 protein recruits viral proteins to AT-rich ori and then unwinds DNA

SV40 large T T is a species-specific DBP/OBP - Pre-initiation complexes do not form in the wrong species - Failure to interact with DNA pol α - primase Binds and sequesters cell cycle regulators - Causes cells to enter S phase

Regulation of DNA synthesis Most of our cells do not divide or do so rarely Viruses do not replicate well in quiescent cells Viruses must induce host replication proteins Done by virus encoded early gene products

Replica*on of DNA Rb protein Cellular retinoblastoma (rb) gene Rb protein controls entry into S Rb loss associated with tumors = tumor suppressor gene

Abrogation of Rb by viral proteins (needed for DNA synthesis, and to pass through cell cycle)