Departments And Divisions
- Department of Pathology & Cell Biology
- Associate Professor of Pathology & Cell Biology
Ribonucleoprotein complexes in post-transcriptional gene regulation and motor neuron disease
Motor control is essential for complex human behaviors such as swallowing, breathing and locomotion. The coordinated activity of motor neurons and their networked neurons and muscle fibers is critical for motor system function and disruption of this network underlies fatal human disorders such as spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS)—the two most common motor neuron diseases of infancy and adulthood, respectively. Importantly, increasing evidence links these diseases to mutations in ubiquitously expressed genes implicated in RNA processing and post-transcriptional gene regulation. However, knowledge of the normal functions of these genes is still limited and the disease mechanisms remain poorly understood. Moreover, a prominent unsolved conundrum common to other neurodegenerative disorders is how disruption of ubiquitously expressed proteins can cause dysfunction or death of specific subsets of neurons. Our work focuses on addressing these fundamental questions using SMA as a paradigm.
SMA is an inherited disorder characterized by degeneration of motor neurons in the spinal cord and atrophy of skeletal muscle, and represents the leading genetic cause of death in infancy. SMA patients are homozygous for deletions or mutations in the survival motor neuron (SMN1) gene, but retain at least one copy of the hypomorphic SMN2 gene. SMN2 produces low levels of full-length SMN protein that cannot compensate for the loss of SMN1, resulting in SMA. Thus, SMA is caused by a ubiquitous deficiency in SMN where remaining levels appear sufficient for function and survival of most cell types, but not of motor neurons. Our previous work helped establish SMN’s essential role in RNA processing. SMN is part of a macromolecular complex that functions in the biogenesis of small nuclear ribonucleoproteins (snRNPs) - which are essential components of the splicing machinery that catalyze intron removal from mRNA precursors in the nucleus - as well as other RNPs. The SMN complex functions as a molecular chaperone to increase the efficiency and specificity of RNP assembly, and to provide an opportunity for RNA-protein interactions to be regulated in vivo.
Research in my laboratory takes advantage of the unique position of SMN at the nexus between RNA regulation and motor neuron biology to advance our understanding of the mechanisms controlling the biogenesis and function of RNPs in post-transcriptional gene regulation and to determine how disruption in these processes contributes to neurodegenerative disease. The underlying logic of our approach is that studies of SMN’s basic functions in RNA regulation will provide the key to understanding disease mechanisms and, conversely, that analysis of motor neuron pathology will uncover new fundamental aspects of SMN biology. To reach this multidisciplinary goal, we employ cell and animal models as well as a wide range of biochemical, molecular and cell biological methodologies. High-throughput screening approaches are also used to identify chemical and genetic modifiers of SMN biology and disease pathways. On one hand, these efforts are designed to increase our knowledge of fundamental mechanisms that control RNA processing and their involvement in motor neuron survival and function. On the other, they aim to deconstruct disease mechanisms and identify potential therapeutic approaches.
- BS, MS, 1992 Biology, Universita degli Studi di Roma
- PhD, 1995 Biotechnology, Universita degli Studi di Roma
Education & Training
- 630 West 168th Street
New York, NY 10032
- (212) 305-3046
- US Patent No: 6,646,113. G. Dreyfuss, U. Fischer, Q. Liu, B. Charroux, L. Pellizzoni. Nucleic acid molecule encoding human survival of motor neuron-interacting protein 1 (SIP1) deletion mutants. Assignee: The Trustees of the University of Pennsylvania. Issue Date: 11/11/2003. International Classifications: C12N; C07H; C07K.
- US Patent No: 7,459,309. G. Dreyfuss, U. Fischer, Q. Liu, B. Charroux, L. Pellizzoni. Isolated polypeptide deletion mutants of survival of motor neuron-interacting protein 1. Assignee: The Trustees of the University of Pennsylvania. Issue Date: 12/02/2008. International Classifications: C07H.
- US Patent Application No: 2009/0156,789. G. Dreyfuss, U. Fischer, Q. Liu, B. Charroux, L. Pellizzoni. Composition, Methods, and Kits Useful for the Diagnosis and Treatment of Spinal Muscular Atrophy. Publication Date: 06/18/2009.
- US Patent Application No: 61/712,220. B.D. McCabe, L. Pellizzoni. Diagnosis and Treatment of SMA and SMN Deficiency. Application Filed: 10/10/2013.
Society for Neuroscience (SFN)
American Society for Cell Biology (ASCB)
American Society for Microbiology (ASM)
Honors & Awards
1992 Laurea Summa Cum Laude, University of Rome La Sapienza
1995 Doctoral Degree in Biotechnology Summa Cum Laude, University of Rome Tor Vergata
2002 Telethon Career Award, Fondazione Telethon
2002 EMBO Young Investigator Award, European Molecular Biology Organization
- RNA biology
- RNA processing
- motor neuron biology and diseases
- molecular mechanisms of neurodegeneration
- synapses and circuits
- cellular/molecular/developmental neuroscience
- Simon, C.M., Janas, A.M., Lotti, F., Tapia, J.C., Pellizzoni, L. & G.Z. Mentis. (2016). A stem cell model of the motor circuit uncouples motor neuron death from hyperexcitability induced by SMN deficiency. Cell Reports, 16, 1416-1430.
- Tisdale, S., Lotti, F., Saieva, L., Van Meerbeke, J.P., Crawford T.O., Sumner, C.J., Mentis, G.Z. & Pellizzoni, L. (2013). SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3’-end formation of histone mRNAs. Cell Reports, 5(5), 1187-1195.
- Lotti, F., Imlach, W.L., Saieva, L., Beck, E.S., Hao, L.T., Li, D.K., Jiao, W., Mentis, G.Z.M., Beattie, C.E., McCabe, B.D. & Pellizzoni, L. (2012). A SMN-dependent U12 splicing event essential for motor circuit function. Cell, 151(2), 440-454.
- Imlach, W.L., Beck, E.S., Choi, B.J., Lotti, F., Pellizzoni, L. & McCabe, B.D. (2012). SMN is Required for sensory-motor circuit function in Drosophila. Cell, 151(2), 427-439.
- Ruggiu, M., McGovern, V.L., Lotti, F., Saieva, L., Li, D.K., Kariya, S., Monani, U.R., Burghes, A.H.M. & Pellizzoni, L. (2012). A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in Spinal Muscular Atrophy. Molecular and Cellular Biology, 32(1), 126 138.
- Gabanella, F., Butchbach, M.E.R., Saieva, L., Carissimi, C., Burghes, A.H. & Pellizzoni, L. (2007). Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs. PLoS ONE, 2(9), e921.
- Gabanella, F., Carissimi, C., Usiello, A. & Pellizzoni, L. (2005). The activity of the Spinal Muscular Atrophy protein is regulated during development and cellular differentiation. Human Molecular Genetics, 14(23), 3629-3642.
- Pellizzoni, L., Yong, J. & Dreyfuss, G. (2002). Essential role for the SMN complex in the specificity of snRNP assembly. Science, 298(5599), 1775-1779.
For a complete list of publications, please visit PubMed.gov