Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

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Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease. / Morgan, Neil; Morris, Mark; Cangul, Hakan; Gleeson, D; Straatman-Iwanowska, Anna; Davies, Nicholas; Keenan, S; Pasha, Shanaz; Rahman, F; Gentle, Dean; Vreeswijk, MPG; Devilee, P; Knowles, MA; Ceylaner, S; Trembath, RC; Dalence, C; Kismet, E; Koseoglu, V; Rossbach, HC; Gissen, Paul; Tannahill, D; Maher, Eamonn.

In: PLoS Genetics, Vol. 6, No. 2, 01.02.2010, p. e1000833.

Research output: Contribution to journalArticle

Harvard

Morgan, N, Morris, M, Cangul, H, Gleeson, D, Straatman-Iwanowska, A, Davies, N, Keenan, S, Pasha, S, Rahman, F, Gentle, D, Vreeswijk, MPG, Devilee, P, Knowles, MA, Ceylaner, S, Trembath, RC, Dalence, C, Kismet, E, Koseoglu, V, Rossbach, HC, Gissen, P, Tannahill, D & Maher, E 2010, 'Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease', PLoS Genetics, vol. 6, no. 2, pp. e1000833. https://doi.org/10.1371/journal.pgen.1000833

APA

Morgan, N., Morris, M., Cangul, H., Gleeson, D., Straatman-Iwanowska, A., Davies, N., Keenan, S., Pasha, S., Rahman, F., Gentle, D., Vreeswijk, MPG., Devilee, P., Knowles, MA., Ceylaner, S., Trembath, RC., Dalence, C., Kismet, E., Koseoglu, V., Rossbach, HC., ... Maher, E. (2010). Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease. PLoS Genetics, 6(2), e1000833. https://doi.org/10.1371/journal.pgen.1000833

Vancouver

Author

Morgan, Neil ; Morris, Mark ; Cangul, Hakan ; Gleeson, D ; Straatman-Iwanowska, Anna ; Davies, Nicholas ; Keenan, S ; Pasha, Shanaz ; Rahman, F ; Gentle, Dean ; Vreeswijk, MPG ; Devilee, P ; Knowles, MA ; Ceylaner, S ; Trembath, RC ; Dalence, C ; Kismet, E ; Koseoglu, V ; Rossbach, HC ; Gissen, Paul ; Tannahill, D ; Maher, Eamonn. / Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease. In: PLoS Genetics. 2010 ; Vol. 6, No. 2. pp. e1000833.

Bibtex

@article{faeb1c74e45f4b6e9c01e40f0d84309b,
title = "Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease",
abstract = "The histiocytoses are a heterogeneous group of disorders characterised by an excessive number of histiocytes. In most cases the pathophysiology is unclear and treatment is nonspecific. Faisalabad histiocytosis (FHC) (MIM 602782) has been classed as an autosomal recessively inherited form of histiocytosis with similarities to Rosai-Dorfman disease (RDD) (also known as sinus histiocytosis with massive lymphadenopathy (SHML)). To elucidate the molecular basis of FHC, we performed autozygosity mapping studies in a large consanguineous family and identified a novel locus at chromosome 10q22.1. Mutation analysis of candidate genes within the target interval identified biallelic germline mutations in SLC29A3 in the FHC kindred and in two families reported to have familial RDD. Analysis of SLC29A3 expression during mouse embryogenesis revealed widespread expression by e14.5 with prominent expression in the central nervous system, eye, inner ear, and epithelial tissues including the gastrointestinal tract. SLC29A3 encodes an intracellular equilibrative nucleoside transporter (hENT3) with affinity for adenosine. Recently germline mutations in SLC29A3 were also described in two rare autosomal recessive disorders with overlapping phenotypes: (a) H syndrome (MIM 612391) that is characterised by cutaneous hyperpigmentation and hypertrichosis, hepatomegaly, heart anomalies, hearing loss, and hypogonadism; and (b) PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus) syndrome. Our findings suggest that a variety of clinical diagnoses (H and PHID syndromes, FHC, and familial RDD) can be included in a new diagnostic category of SLC29A3 spectrum disorder.",
keywords = "genetics, Renal cell carcinoma, hypoxia-inducible factors, VHL",
author = "Neil Morgan and Mark Morris and Hakan Cangul and D Gleeson and Anna Straatman-Iwanowska and Nicholas Davies and S Keenan and Shanaz Pasha and F Rahman and Dean Gentle and MPG Vreeswijk and P Devilee and MA Knowles and S Ceylaner and RC Trembath and C Dalence and E Kismet and V Koseoglu and HC Rossbach and Paul Gissen and D Tannahill and Eamonn Maher",
year = "2010",
month = feb
day = "1",
doi = "10.1371/journal.pgen.1000833",
language = "English",
volume = "6",
pages = "e1000833",
journal = "PLoS Genetics",
issn = "1553-7390",
publisher = "Public Library of Science (PLOS)",
number = "2",

}

RIS

TY - JOUR

T1 - Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

AU - Morgan, Neil

AU - Morris, Mark

AU - Cangul, Hakan

AU - Gleeson, D

AU - Straatman-Iwanowska, Anna

AU - Davies, Nicholas

AU - Keenan, S

AU - Pasha, Shanaz

AU - Rahman, F

AU - Gentle, Dean

AU - Vreeswijk, MPG

AU - Devilee, P

AU - Knowles, MA

AU - Ceylaner, S

AU - Trembath, RC

AU - Dalence, C

AU - Kismet, E

AU - Koseoglu, V

AU - Rossbach, HC

AU - Gissen, Paul

AU - Tannahill, D

AU - Maher, Eamonn

PY - 2010/2/1

Y1 - 2010/2/1

N2 - The histiocytoses are a heterogeneous group of disorders characterised by an excessive number of histiocytes. In most cases the pathophysiology is unclear and treatment is nonspecific. Faisalabad histiocytosis (FHC) (MIM 602782) has been classed as an autosomal recessively inherited form of histiocytosis with similarities to Rosai-Dorfman disease (RDD) (also known as sinus histiocytosis with massive lymphadenopathy (SHML)). To elucidate the molecular basis of FHC, we performed autozygosity mapping studies in a large consanguineous family and identified a novel locus at chromosome 10q22.1. Mutation analysis of candidate genes within the target interval identified biallelic germline mutations in SLC29A3 in the FHC kindred and in two families reported to have familial RDD. Analysis of SLC29A3 expression during mouse embryogenesis revealed widespread expression by e14.5 with prominent expression in the central nervous system, eye, inner ear, and epithelial tissues including the gastrointestinal tract. SLC29A3 encodes an intracellular equilibrative nucleoside transporter (hENT3) with affinity for adenosine. Recently germline mutations in SLC29A3 were also described in two rare autosomal recessive disorders with overlapping phenotypes: (a) H syndrome (MIM 612391) that is characterised by cutaneous hyperpigmentation and hypertrichosis, hepatomegaly, heart anomalies, hearing loss, and hypogonadism; and (b) PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus) syndrome. Our findings suggest that a variety of clinical diagnoses (H and PHID syndromes, FHC, and familial RDD) can be included in a new diagnostic category of SLC29A3 spectrum disorder.

AB - The histiocytoses are a heterogeneous group of disorders characterised by an excessive number of histiocytes. In most cases the pathophysiology is unclear and treatment is nonspecific. Faisalabad histiocytosis (FHC) (MIM 602782) has been classed as an autosomal recessively inherited form of histiocytosis with similarities to Rosai-Dorfman disease (RDD) (also known as sinus histiocytosis with massive lymphadenopathy (SHML)). To elucidate the molecular basis of FHC, we performed autozygosity mapping studies in a large consanguineous family and identified a novel locus at chromosome 10q22.1. Mutation analysis of candidate genes within the target interval identified biallelic germline mutations in SLC29A3 in the FHC kindred and in two families reported to have familial RDD. Analysis of SLC29A3 expression during mouse embryogenesis revealed widespread expression by e14.5 with prominent expression in the central nervous system, eye, inner ear, and epithelial tissues including the gastrointestinal tract. SLC29A3 encodes an intracellular equilibrative nucleoside transporter (hENT3) with affinity for adenosine. Recently germline mutations in SLC29A3 were also described in two rare autosomal recessive disorders with overlapping phenotypes: (a) H syndrome (MIM 612391) that is characterised by cutaneous hyperpigmentation and hypertrichosis, hepatomegaly, heart anomalies, hearing loss, and hypogonadism; and (b) PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus) syndrome. Our findings suggest that a variety of clinical diagnoses (H and PHID syndromes, FHC, and familial RDD) can be included in a new diagnostic category of SLC29A3 spectrum disorder.

KW - genetics

KW - Renal cell carcinoma

KW - hypoxia-inducible factors

KW - VHL

U2 - 10.1371/journal.pgen.1000833

DO - 10.1371/journal.pgen.1000833

M3 - Article

C2 - 20140240

VL - 6

SP - e1000833

JO - PLoS Genetics

JF - PLoS Genetics

SN - 1553-7390

IS - 2

ER -