Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

Stefan Gräf; Matthias Haimel; Marta Bleda; Charaka Hadinnapola; Laura Southgate; Wei Li; Joshua Hodgson; Bin Liu; Richard M. Salmon; Mark Southwood; Rajiv D. Machado; Jennifer M. Martin; Carmen M. Treacy; Katherine Yates; Louise C. Daugherty; Olga Shamardina; Deborah Whitehorn; Simon Holden; Micheala Aldred; Harm J. Bogaard; Colin Church; Gerry Coghlan; Robin Condliffe; Paul A. Corris; Cesare Danesino; Mélanie Eyries; Henning Gall; Stefano Ghio; Hossein-ardeschir Ghofrani; J. Simon R. Gibbs; Barbara Girerd; Arjan C. Houweling; Luke Howard; Marc Humbert; David G. Kiely; Gabor Kovacs; Robert V. Mackenzie Ross; Shahin Moledina; David Montani; Michael Newnham; Andrea Olschewski; Horst Olschewski; Andrew J. Peacock; Joanna Pepke-zaba; Inga Prokopenko; Christopher J. Rhodes; Laura Scelsi; Werner Seeger; Florent Soubrier; Dan F. Stein; Jay Suntharalingam; Emilia M. Swietlik; Mark R. Toshner; David A. Van Heel; Anton Vonk Noordegraaf; Quinten Waisfisz; John Wharton; Stephen J. Wort; Willem H. Ouwehand; Nicole Soranzo; Allan Lawrie; Paul D. Upton; Martin R. Wilkins; Richard C. Trembath; Nicholas W. Morrell

doi:10.1038/s41467-018-03672-4

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

Stefan Gräf, Matthias Haimel, Marta Bleda, Charaka Hadinnapola, Laura Southgate, Wei Li, Joshua Hodgson, Bin Liu, Richard M. Salmon, Mark Southwood, Rajiv D. Machado, Jennifer M. Martin, Carmen M. Treacy, Katherine Yates, Louise C. Daugherty, Olga Shamardina, Deborah Whitehorn, Simon Holden, Micheala Aldred, Harm J. BogaardColin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Cesare Danesino, Mélanie Eyries, Henning Gall, Stefano Ghio, Hossein-ardeschir Ghofrani, J. Simon R. Gibbs, Barbara Girerd, Arjan C. Houweling, Luke Howard, Marc Humbert, David G. Kiely, Gabor Kovacs, Robert V. Mackenzie Ross, Shahin Moledina, David Montani, Michael Newnham, Andrea Olschewski, Horst Olschewski, Andrew J. Peacock, Joanna Pepke-zaba, Inga Prokopenko, Christopher J. Rhodes, Laura Scelsi, Werner Seeger, Florent Soubrier, Dan F. Stein, Jay Suntharalingam, Emilia M. Swietlik, Mark R. Toshner, David A. Van Heel, Anton Vonk Noordegraaf, Quinten Waisfisz, John Wharton, Stephen J. Wort, Willem H. Ouwehand, Nicole Soranzo, Allan Lawrie, Paul D. Upton, Martin R. Wilkins, Richard C. Trembath, Nicholas W. Morrell

Applied Health Research

Research output: Contribution to journal › Article › peer-review

124 Citations (Scopus)

185 Downloads (Pure)

Abstract

Pulmonary arterial hypertension (PAH) is a rare disorder with a poor prognosis. Deleterious variation within components of the transforming growth factor-β pathway, particularly the bone morphogenetic protein type 2 receptor (BMPR2), underlies most heritable forms of PAH. To identify the missing heritability we perform whole-genome sequencing in 1038 PAH index cases and 6385 PAH-negative control subjects. Case-control analyses reveal significant overrepresentation of rare variants in ATP13A3, AQP1 and SOX17, and provide independent validation of a critical role for GDF2 in PAH. We demonstrate familial segregation of mutations in SOX17 and AQP1 with PAH. Mutations in GDF2, encoding a BMPR2 ligand, lead to reduced secretion from transfected cells. In addition, we identify pathogenic mutations in the majority of previously reported PAH genes, and provide evidence for further putative genes. Taken together these findings contribute new insights into the molecular basis of PAH and indicate unexplored pathways for therapeutic intervention.

Original language	English
Article number	1416
Number of pages	16
Journal	Nature Communications
Volume	9
Issue number	1
DOIs	https://doi.org/10.1038/s41467-018-03672-4
Publication status	Published - 12 Apr 2018

Access to Document

10.1038/s41467-018-03672-4Licence: Creative Commons: Attribution (CC BY)

S_Gräf_et_al_Identification_of_rare_sequence_variation_Nature_Communications_2018
Checked for eligibility: 07/01/2018
Final published version, 7.28 MBLicence: Creative Commons: Attribution (CC BY)

http://www.nature.com/articles/s41467-018-03672-4Licence: Creative Commons: Attribution (CC BY)

Cite this

Gräf, S., Haimel, M., Bleda, M., Hadinnapola, C., Southgate, L., Li, W., Hodgson, J., Liu, B., Salmon, R. M., Southwood, M., Machado, R. D., Martin, J. M., Treacy, C. M., Yates, K., Daugherty, L. C., Shamardina, O., Whitehorn, D., Holden, S., Aldred, M., ... Morrell, N. W. (2018). Identification of rare sequence variation underlying heritable pulmonary arterial hypertension. Nature Communications, 9(1), Article 1416. https://doi.org/10.1038/s41467-018-03672-4

@article{57f81cfa2ac448a095981e33c5770aa5,

title = "Identification of rare sequence variation underlying heritable pulmonary arterial hypertension",

abstract = "Pulmonary arterial hypertension (PAH) is a rare disorder with a poor prognosis. Deleterious variation within components of the transforming growth factor-β pathway, particularly the bone morphogenetic protein type 2 receptor (BMPR2), underlies most heritable forms of PAH. To identify the missing heritability we perform whole-genome sequencing in 1038 PAH index cases and 6385 PAH-negative control subjects. Case-control analyses reveal significant overrepresentation of rare variants in ATP13A3, AQP1 and SOX17, and provide independent validation of a critical role for GDF2 in PAH. We demonstrate familial segregation of mutations in SOX17 and AQP1 with PAH. Mutations in GDF2, encoding a BMPR2 ligand, lead to reduced secretion from transfected cells. In addition, we identify pathogenic mutations in the majority of previously reported PAH genes, and provide evidence for further putative genes. Taken together these findings contribute new insights into the molecular basis of PAH and indicate unexplored pathways for therapeutic intervention.",

author = "Stefan Gr{\"a}f and Matthias Haimel and Marta Bleda and Charaka Hadinnapola and Laura Southgate and Wei Li and Joshua Hodgson and Bin Liu and Salmon, {Richard M.} and Mark Southwood and Machado, {Rajiv D.} and Martin, {Jennifer M.} and Treacy, {Carmen M.} and Katherine Yates and Daugherty, {Louise C.} and Olga Shamardina and Deborah Whitehorn and Simon Holden and Micheala Aldred and Bogaard, {Harm J.} and Colin Church and Gerry Coghlan and Robin Condliffe and Corris, {Paul A.} and Cesare Danesino and M{\'e}lanie Eyries and Henning Gall and Stefano Ghio and Hossein-ardeschir Ghofrani and Gibbs, {J. Simon R.} and Barbara Girerd and Houweling, {Arjan C.} and Luke Howard and Marc Humbert and Kiely, {David G.} and Gabor Kovacs and {Mackenzie Ross}, {Robert V.} and Shahin Moledina and David Montani and Michael Newnham and Andrea Olschewski and Horst Olschewski and Peacock, {Andrew J.} and Joanna Pepke-zaba and Inga Prokopenko and Rhodes, {Christopher J.} and Laura Scelsi and Werner Seeger and Florent Soubrier and Stein, {Dan F.} and Jay Suntharalingam and Swietlik, {Emilia M.} and Toshner, {Mark R.} and {Van Heel}, {David A.} and {Vonk Noordegraaf}, Anton and Quinten Waisfisz and John Wharton and Wort, {Stephen J.} and Ouwehand, {Willem H.} and Nicole Soranzo and Allan Lawrie and Upton, {Paul D.} and Wilkins, {Martin R.} and Trembath, {Richard C.} and Morrell, {Nicholas W.}",

year = "2018",

month = apr,

day = "12",

doi = "10.1038/s41467-018-03672-4",

language = "English",

volume = "9",

journal = "Nature Communications",

issn = "2041-1723",

publisher = "Springer",

number = "1",

}

Gräf, S, Haimel, M, Bleda, M, Hadinnapola, C, Southgate, L, Li, W, Hodgson, J, Liu, B, Salmon, RM, Southwood, M, Machado, RD, Martin, JM, Treacy, CM, Yates, K, Daugherty, LC, Shamardina, O, Whitehorn, D, Holden, S, Aldred, M, Bogaard, HJ, Church, C, Coghlan, G, Condliffe, R, Corris, PA, Danesino, C, Eyries, M, Gall, H, Ghio, S, Ghofrani, H, Gibbs, JSR, Girerd, B, Houweling, AC, Howard, L, Humbert, M, Kiely, DG, Kovacs, G, Mackenzie Ross, RV, Moledina, S, Montani, D, Newnham, M, Olschewski, A, Olschewski, H, Peacock, AJ, Pepke-zaba, J, Prokopenko, I, Rhodes, CJ, Scelsi, L, Seeger, W, Soubrier, F, Stein, DF, Suntharalingam, J, Swietlik, EM, Toshner, MR, Van Heel, DA, Vonk Noordegraaf, A, Waisfisz, Q, Wharton, J, Wort, SJ, Ouwehand, WH, Soranzo, N, Lawrie, A, Upton, PD, Wilkins, MR, Trembath, RC & Morrell, NW 2018, 'Identification of rare sequence variation underlying heritable pulmonary arterial hypertension', Nature Communications, vol. 9, no. 1, 1416. https://doi.org/10.1038/s41467-018-03672-4

TY - JOUR

T1 - Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

AU - Gräf, Stefan

AU - Haimel, Matthias

AU - Bleda, Marta

AU - Hadinnapola, Charaka

AU - Southgate, Laura

AU - Li, Wei

AU - Hodgson, Joshua

AU - Liu, Bin

AU - Salmon, Richard M.

AU - Southwood, Mark

AU - Machado, Rajiv D.

AU - Martin, Jennifer M.

AU - Treacy, Carmen M.

AU - Yates, Katherine

AU - Daugherty, Louise C.

AU - Shamardina, Olga

AU - Whitehorn, Deborah

AU - Holden, Simon

AU - Aldred, Micheala

AU - Bogaard, Harm J.

AU - Church, Colin

AU - Coghlan, Gerry

AU - Condliffe, Robin

AU - Corris, Paul A.

AU - Danesino, Cesare

AU - Eyries, Mélanie

AU - Gall, Henning

AU - Ghio, Stefano

AU - Ghofrani, Hossein-ardeschir

AU - Gibbs, J. Simon R.

AU - Girerd, Barbara

AU - Houweling, Arjan C.

AU - Howard, Luke

AU - Humbert, Marc

AU - Kiely, David G.

AU - Kovacs, Gabor

AU - Mackenzie Ross, Robert V.

AU - Moledina, Shahin

AU - Montani, David

AU - Newnham, Michael

AU - Olschewski, Andrea

AU - Olschewski, Horst

AU - Peacock, Andrew J.

AU - Pepke-zaba, Joanna

AU - Prokopenko, Inga

AU - Rhodes, Christopher J.

AU - Scelsi, Laura

AU - Seeger, Werner

AU - Soubrier, Florent

AU - Stein, Dan F.

AU - Suntharalingam, Jay

AU - Swietlik, Emilia M.

AU - Toshner, Mark R.

AU - Van Heel, David A.

AU - Vonk Noordegraaf, Anton

AU - Waisfisz, Quinten

AU - Wharton, John

AU - Wort, Stephen J.

AU - Ouwehand, Willem H.

AU - Soranzo, Nicole

AU - Lawrie, Allan

AU - Upton, Paul D.

AU - Wilkins, Martin R.

AU - Trembath, Richard C.

AU - Morrell, Nicholas W.

PY - 2018/4/12

Y1 - 2018/4/12

N2 - Pulmonary arterial hypertension (PAH) is a rare disorder with a poor prognosis. Deleterious variation within components of the transforming growth factor-β pathway, particularly the bone morphogenetic protein type 2 receptor (BMPR2), underlies most heritable forms of PAH. To identify the missing heritability we perform whole-genome sequencing in 1038 PAH index cases and 6385 PAH-negative control subjects. Case-control analyses reveal significant overrepresentation of rare variants in ATP13A3, AQP1 and SOX17, and provide independent validation of a critical role for GDF2 in PAH. We demonstrate familial segregation of mutations in SOX17 and AQP1 with PAH. Mutations in GDF2, encoding a BMPR2 ligand, lead to reduced secretion from transfected cells. In addition, we identify pathogenic mutations in the majority of previously reported PAH genes, and provide evidence for further putative genes. Taken together these findings contribute new insights into the molecular basis of PAH and indicate unexplored pathways for therapeutic intervention.

AB - Pulmonary arterial hypertension (PAH) is a rare disorder with a poor prognosis. Deleterious variation within components of the transforming growth factor-β pathway, particularly the bone morphogenetic protein type 2 receptor (BMPR2), underlies most heritable forms of PAH. To identify the missing heritability we perform whole-genome sequencing in 1038 PAH index cases and 6385 PAH-negative control subjects. Case-control analyses reveal significant overrepresentation of rare variants in ATP13A3, AQP1 and SOX17, and provide independent validation of a critical role for GDF2 in PAH. We demonstrate familial segregation of mutations in SOX17 and AQP1 with PAH. Mutations in GDF2, encoding a BMPR2 ligand, lead to reduced secretion from transfected cells. In addition, we identify pathogenic mutations in the majority of previously reported PAH genes, and provide evidence for further putative genes. Taken together these findings contribute new insights into the molecular basis of PAH and indicate unexplored pathways for therapeutic intervention.

U2 - 10.1038/s41467-018-03672-4

DO - 10.1038/s41467-018-03672-4

M3 - Article

SN - 2041-1723

VL - 9

JO - Nature Communications

JF - Nature Communications

IS - 1

M1 - 1416

ER -

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

Abstract

Access to Document

Fingerprint

Cite this