Our research program centers on achieving a comprehensive molecular understanding of human polycystic liver and kidney disease. Our goal is discovery novel paradigms for effective treatment of patients. We have taken an approach that begins with disease gene discovery through positional cloning to understand the genetic bases for the diseases, followed by functional studies to understand cellular pathogenesis. Under the current grant, we recruited patients with isolated autosomal dominant polycystic liver disease (ADPLD;MIM 174050) and completed a comprehensive clinical characterization of the disease. We established genetic linkage for one locus, PLD1, and discovered the disease gene, PRKCSH. We identified a second locus for ADPLD on chromosome 6 and identified human SEC63 as PLD2. Mutations in these genes account for ~ 25% of ADPLD probands in our cohort and suggest that there is at least one additional locus, PLD3, for ADPLD. PRKCSH encodes the B-subunit of glucosidase II (GIIB), a glucose trimming enzyme involved in protein maturation and quality control in the ER. SEC63 encodes a component of the ER protein translocation machinery that functions in concert with GII to achieve proper topology and folding of integral membrane or secreted glycoproteins. This proposal seeks to further define cellular pathways to cyst formation by discovery of additional genes involved in ADPLD, by determining whether two hits are required for cyst formation in ADPLD, and by defining the relationship between protein maturation in the ER and the normal function of primary cilia in bile duct epithelium. We propose to identify additional genes (e.g., PLD3) responsible for ADPLD by use of a combination of """"""""classical"""""""" positional cloning and candidate gene approaches. We will use mouse models to test the hypothesis that cyst formation in ADPLD requires somatic second hits as is the case in ADPKD. We will determine whether Prkcsh and Sec63 mutations result in improper maturation and cilial delivery of the Pkd 1, Pkd2 and Pkhd 1 gene products. These studies will improve our understanding of the cellular and molecular bases of polycystic diseases by using the novel entry points into the pathogenic pathways made possible by our discovery of PRKCSH and SEC63 as disease genes. At the same time, we will improve our understanding of ADPLD as a disease condition and develop insights that will help patients affected by this condition.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
3R01DK051041-12S1
Application #
7863853
Study Section
Hepatobiliary Pathophysiology Study Section (HBPP)
Program Officer
Karp, Robert W
Project Start
2009-07-20
Project End
2010-05-31
Budget Start
2009-07-20
Budget End
2010-05-31
Support Year
12
Fiscal Year
2009
Total Cost
$8,656
Indirect Cost
Name
Yale University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Besse, Whitney; Choi, Jungmin; Ahram, Dina et al. (2018) A noncoding variant in GANAB explains isolated polycystic liver disease (PCLD) in a large family. Hum Mutat 39:378-382
Ma, Ming; Gallagher, Anna-Rachel; Somlo, Stefan (2017) Ciliary Mechanisms of Cyst Formation in Polycystic Kidney Disease. Cold Spring Harb Perspect Biol 9:
Besse, Whitney; Dong, Ke; Choi, Jungmin et al. (2017) Isolated polycystic liver disease genes define effectors of polycystin-1 function. J Clin Invest 127:1772-1785
Hassan, Hossam; Tian, Xuefei; Inoue, Kazunori et al. (2016) Essential Role of X-Box Binding Protein-1 during Endoplasmic Reticulum Stress in Podocytes. J Am Soc Nephrol 27:1055-65
Pema, Monika; Drusian, Luca; Chiaravalli, Marco et al. (2016) mTORC1-mediated inhibition of polycystin-1 expression drives renal cyst formation in tuberous sclerosis complex. Nat Commun 7:10786
Fedeles, Sorin V; So, Jae-Seon; Shrikhande, Amol et al. (2015) Sec63 and Xbp1 regulate IRE1? activity and polycystic disease severity. J Clin Invest 125:1955-67
Fedeles, Sorin V; Gallagher, Anna-Rachel; Somlo, Stefan (2014) Polycystin-1: a master regulator of intersecting cystic pathways. Trends Mol Med 20:251-60
Hofherr, Alexis; Wagner, Claudius; Fedeles, Sorin et al. (2014) N-glycosylation determines the abundance of the transient receptor potential channel TRPP2. J Biol Chem 289:14854-67
Cai, Yiqiang; Fedeles, Sorin V; Dong, Ke et al. (2014) Altered trafficking and stability of polycystins underlie polycystic kidney disease. J Clin Invest 124:5129-44
Ma, Ming; Tian, Xin; Igarashi, Peter et al. (2013) Loss of cilia suppresses cyst growth in genetic models of autosomal dominant polycystic kidney disease. Nat Genet 45:1004-12

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