It has become increasingly clear that, in vivo, RNA processing events occur co-transcriptionally, mediated by RNA processing factors associated with the carboxy-terminal domain (CTD) of the elongating RNA pol II complex. It would be expected that viral regulators of gene expression would influence this process, however, few examples of such viral regulators have so far been identified. We have recently demonstrated that in the presence of adenovirus type 5 (Ad5), the large Rep protein of adeno-associated virus type 2 (AAV2), a member of the Parvoviridae Family, acts as a co-transcriptional trans-regulator of RNA processing. We propose to further characterize this novel activity of Rep in Specific Aim I, by: 1.determining the cis-acting signals in the AAV2 transcription unit that are required and sufficient to be responsive to the RNA processing effects of Rep and Ad5; 2.determining the trans-acting helper functions that are required to support Rep's effect, and by determining the domains of the Rep protein that mediate its RNA processing effect; and 3.determining the mechanism of Rep's co-transcriptional effect on processing of AAV2 RNA. Specifically, we will test our model that Rep alters the composition of RNA processing factors associated with the CTD of the elongating transcription complex. Our survey of the transcription profile of the other AAV serotypes has revealed that RNA produced from AAV5 efficiently utilizes a polyadenylation site, (pA) p, within the viral intron. The usage of (pA) p is directly proportional to the distance between the promoter and that site, and (pA) p is subject to inhibition by an upstream intron donor. This will be further characterized in Specific Aim 2, by: 1.characterizing the cis-and trans-acting determinants that govern the alternative polyadenylation of AAV5 RNA; 2.determining why RNAs generated from the upstream P7 promoter utilize (pA) p, and those from nearby P41 read through; and 3.examining the consequences of internal polyadenylation for the AAV5 life cycle. These aspects of gene expression are critically important features of AAV biology. Also, as both of these RNA processing functions are probably best understood in a co-transcriptional framework, their characterization in the tractable AAV system will help illuminate this new paradigm of gene expression. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI056310-04
Application #
7174639
Study Section
Virology Study Section (VR)
Program Officer
Park, Eun-Chung
Project Start
2004-02-01
Project End
2009-01-31
Budget Start
2007-02-01
Budget End
2008-01-31
Support Year
4
Fiscal Year
2007
Total Cost
$277,583
Indirect Cost
Name
University of Missouri-Columbia
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
153890272
City
Columbia
State
MO
Country
United States
Zip Code
65211
Li, Long; Pintel, David J (2012) Splicing of goose parvovirus pre-mRNA influences cytoplasmic translation of the processed mRNA. Virology 426:60-5
Venkatesh, Lakshminarayan K; Fasina, Olufemi; Pintel, David J (2012) RNAse mapping and quantitation of RNA isoforms. Methods Mol Biol 883:121-9
Farris, K David; Pintel, David J (2010) Adeno-associated virus type 5 utilizes alternative translation initiation to encode a small Rep40-like protein. J Virol 84:1193-7
Farris, K David; Fasina, Olufemi; Sukhu, Loretta et al. (2010) Adeno-associated virus small rep proteins are modified with at least two types of polyubiquitination. J Virol 84:1206-11
Li, Long; Qiu, Jianming; Pintel, David J (2009) The choice of translation initiation site of the rep proteins from goose parvovirus P9-generated mRNA is governed by splicing and the nature of the excised intron. J Virol 83:10264-8
Farris, K David; Pintel, David J (2008) Improved splicing of adeno-associated viral (AAV) capsid protein-supplying pre-mRNAs leads to increased recombinant AAV vector production. Hum Gene Ther 19:1421-7
Lin, Feng; Guan, Wuxiang; Cheng, Fang et al. (2008) ELISAs using human bocavirus VP2 virus-like particles for detection of antibodies against HBoV. J Virol Methods 149:110-7
Ye, Chaoyang; Pintel, David J (2008) The transcription strategy of bovine adeno-associated virus (B-AAV) combines features of both adeno-associated virus type 2 (AAV2) and type 5 (AAV5). Virology 370:392-402
Guan, Wuxiang; Cheng, Fang; Yoto, Yuko et al. (2008) Block to the production of full-length B19 virus transcripts by internal polyadenylation is overcome by replication of the viral genome. J Virol 82:9951-63
Nayak, Ramnath; Farris, K David; Pintel, David J (2008) E4Orf6-E1B-55k-dependent degradation of de novo-generated adeno-associated virus type 5 Rep52 and capsid proteins employs a cullin 5-containing E3 ligase complex. J Virol 82:3803-8

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