Spatial and temporal expression of immunoglobulin superfamily member 1 in the rat

Loss-of-function mutations in the immunoglobulin superfamily member 1 (IGSF1) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism, variable prolactin and GH deficiency, delayed pubertal testosterone rise, and obesity. To understand the pathophysiology of this syndrome, knowledg...

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Published inJournal of endocrinology Vol. 226; no. 3; pp. 181 - 191
Main Authors Joustra, Sjoerd D, Meijer, Onno C, Heinen, Charlotte A, Mol, Isabel M, Laghmani, El Houari, Sengers, Rozemarijn M A, Carreno, Gabriela, van Trotsenburg, A S Paul, Biermasz, Nienke R, Bernard, Daniel J, Wit, Jan M, Oostdijk, Wilma, van Pelt, Ans M M, Hamer, Geert, Wagenaar, Gerry T M
Format Journal Article
LanguageEnglish
Published England Bioscientifica Ltd 01.09.2015
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Online AccessGet full text
ISSN0022-0795
1479-6805
1479-6805
DOI10.1530/JOE-15-0204

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Abstract Loss-of-function mutations in the immunoglobulin superfamily member 1 (IGSF1) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism, variable prolactin and GH deficiency, delayed pubertal testosterone rise, and obesity. To understand the pathophysiology of this syndrome, knowledge on IGSF1's place in normal development is imperative. Therefore, we investigated spatial and temporal protein and mRNA expression of IGSF1 in rats using immunohistochemistry, real-time quantitative PCR (qPCR), and in situ hybridization. We observed high levels of IGSF1 expression in the brain, specifically the embryonic and adult choroid plexus and hypothalamus (principally in glial cells), and in the pituitary gland (PIT1-lineage of GH, TSH, and PRL-producing cells). IGSF1 is also expressed in the embryonic and adult zona glomerulosa of the adrenal gland, islets of Langerhans of the pancreas, and costameres of the heart and skeletal muscle. IGSF1 is highly expressed in fetal liver, but is absent shortly after birth. In the adult testis, IGSF1 is present in Sertoli cells (epithelial stages XIII–VI), and elongating spermatids (stages X–XII). Specificity of protein expression was corroborated with Igsf1 mRNA expression in all tissues. The expression patterns of IGSF1 in the pituitary gland and testis are consistent with the pituitary hormone deficiencies and macroorchidism observed in patients with IGSF1 deficiency. The expression in the brain, adrenal gland, pancreas, liver, and muscle suggest IGSF1's function in endocrine physiology might be more extensive than previously considered.
AbstractList Loss-of-function mutations in the immunoglobulin superfamily member 1 (IGSF1) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism, variable prolactin and GH deficiency, delayed pubertal testosterone rise, and obesity. To understand the pathophysiology of this syndrome, knowledge on IGSF1's place in normal development is imperative. Therefore, we investigated spatial and temporal protein and mRNA expression of IGSF1 in rats using immunohistochemistry, real-time quantitative PCR (qPCR), and in situ hybridization. We observed high levels of IGSF1 expression in the brain, specifically the embryonic and adult choroid plexus and hypothalamus (principally in glial cells), and in the pituitary gland (PIT1-lineage of GH, TSH, and PRL-producing cells). IGSF1 is also expressed in the embryonic and adult zona glomerulosa of the adrenal gland, islets of Langerhans of the pancreas, and costameres of the heart and skeletal muscle. IGSF1 is highly expressed in fetal liver, but is absent shortly after birth. In the adult testis, IGSF1 is present in Sertoli cells (epithelial stages XIII-VI), and elongating spermatids (stages X-XII). Specificity of protein expression was corroborated with Igsf1 mRNA expression in all tissues. The expression patterns of IGSF1 in the pituitary gland and testis are consistent with the pituitary hormone deficiencies and macroorchidism observed in patients with IGSF1 deficiency. The expression in the brain, adrenal gland, pancreas, liver, and muscle suggest IGSF1's function in endocrine physiology might be more extensive than previously considered.
Loss-of-function mutations in the immunoglobulin superfamily member 1 (IGSF1) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism, variable prolactin and GH deficiency, delayed pubertal testosterone rise, and obesity. To understand the pathophysiology of this syndrome, knowledge on IGSF1's place in normal development is imperative. Therefore, we investigated spatial and temporal protein and mRNA expression of IGSF1 in rats using immunohistochemistry, real-time quantitative PCR (qPCR), and in situ hybridization. We observed high levels of IGSF1 expression in the brain, specifically the embryonic and adult choroid plexus and hypothalamus (principally in glial cells), and in the pituitary gland (PIT1-lineage of GH, TSH, and PRL-producing cells). IGSF1 is also expressed in the embryonic and adult zona glomerulosa of the adrenal gland, islets of Langerhans of the pancreas, and costameres of the heart and skeletal muscle. IGSF1 is highly expressed in fetal liver, but is absent shortly after birth. In the adult testis, IGSF1 is present in Sertoli cells (epithelial stages XIII-VI), and elongating spermatids (stages X-XII). Specificity of protein expression was corroborated with Igsf1 mRNA expression in all tissues. The expression patterns of IGSF1 in the pituitary gland and testis are consistent with the pituitary hormone deficiencies and macroorchidism observed in patients with IGSF1 deficiency. The expression in the brain, adrenal gland, pancreas, liver, and muscle suggest IGSF1's function in endocrine physiology might be more extensive than previously considered.Loss-of-function mutations in the immunoglobulin superfamily member 1 (IGSF1) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism, variable prolactin and GH deficiency, delayed pubertal testosterone rise, and obesity. To understand the pathophysiology of this syndrome, knowledge on IGSF1's place in normal development is imperative. Therefore, we investigated spatial and temporal protein and mRNA expression of IGSF1 in rats using immunohistochemistry, real-time quantitative PCR (qPCR), and in situ hybridization. We observed high levels of IGSF1 expression in the brain, specifically the embryonic and adult choroid plexus and hypothalamus (principally in glial cells), and in the pituitary gland (PIT1-lineage of GH, TSH, and PRL-producing cells). IGSF1 is also expressed in the embryonic and adult zona glomerulosa of the adrenal gland, islets of Langerhans of the pancreas, and costameres of the heart and skeletal muscle. IGSF1 is highly expressed in fetal liver, but is absent shortly after birth. In the adult testis, IGSF1 is present in Sertoli cells (epithelial stages XIII-VI), and elongating spermatids (stages X-XII). Specificity of protein expression was corroborated with Igsf1 mRNA expression in all tissues. The expression patterns of IGSF1 in the pituitary gland and testis are consistent with the pituitary hormone deficiencies and macroorchidism observed in patients with IGSF1 deficiency. The expression in the brain, adrenal gland, pancreas, liver, and muscle suggest IGSF1's function in endocrine physiology might be more extensive than previously considered.
Loss-of-function mutations in the immunoglobulin superfamily member 1 ( IGSF1 ) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism, variable prolactin and GH deficiency, delayed pubertal testosterone rise, and obesity. To understand the pathophysiology of this syndrome, knowledge on IGSF1's place in normal development is imperative. Therefore, we investigated spatial and temporal protein and mRNA expression of IGSF1 in rats using immunohistochemistry, real-time quantitative PCR (qPCR), and in situ hybridization. We observed high levels of IGSF1 expression in the brain, specifically the embryonic and adult choroid plexus and hypothalamus (principally in glial cells), and in the pituitary gland (PIT1-lineage of GH, TSH, and PRL-producing cells). IGSF1 is also expressed in the embryonic and adult zona glomerulosa of the adrenal gland, islets of Langerhans of the pancreas, and costameres of the heart and skeletal muscle. IGSF1 is highly expressed in fetal liver, but is absent shortly after birth. In the adult testis, IGSF1 is present in Sertoli cells (epithelial stages XIII–VI), and elongating spermatids (stages X–XII). Specificity of protein expression was corroborated with Igsf1 mRNA expression in all tissues. The expression patterns of IGSF1 in the pituitary gland and testis are consistent with the pituitary hormone deficiencies and macroorchidism observed in patients with IGSF1 deficiency. The expression in the brain, adrenal gland, pancreas, liver, and muscle suggest IGSF1's function in endocrine physiology might be more extensive than previously considered.
Author Joustra, Sjoerd D
Sengers, Rozemarijn M A
Carreno, Gabriela
van Pelt, Ans M M
Bernard, Daniel J
Wagenaar, Gerry T M
Mol, Isabel M
Meijer, Onno C
Biermasz, Nienke R
Laghmani, El Houari
Wit, Jan M
van Trotsenburg, A S Paul
Hamer, Geert
Heinen, Charlotte A
Oostdijk, Wilma
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Cites_doi 10.1073/pnas.0400782101
10.1210/me.15.4.654
10.1097/00006676-199001000-00005
10.1038/nature11405
10.1210/er.2012-1076
10.1186/1741-7007-6-49
10.1016/j.ygeno.2005.04.008
10.1210/en.2011-0109
10.1093/nar/29.9.e45
10.1016/S0021-9258(18)98767-3
10.1007/BF02738704
10.1210/endo-112-3-951
10.1152/ajplung.00360.2012
10.1210/me.15.4.668
10.1074/jbc.R200021200
10.1530/eje.1.01937
10.1007/978-3-540-89979-2_3
10.1677/joe.0.1820055
10.1111/j.1365-2826.2008.01676.x
10.1128/MCB.23.14.4882-4891.2003
10.1073/pnas.94.20.10862
10.1210/er.2013-1087
10.1159/000164066
10.1210/jc.2013-2743
10.1006/geno.1997.5156
10.1016/S0378-1119(98)00253-4
10.1007/BF00130513
10.1210/edrv-3-4-404
10.1016/j.freeradbiomed.2003.12.007
10.1074/jbc.M807527200
10.1038/ng.2453
10.1186/1471-2164-10-269
10.1210/jc.2012-1616
10.1210/en.141.7.2600
10.1210/en.132.3.1207
10.1055/s-2007-978911
10.1038/sj.onc.1208479
10.1073/pnas.012025199
10.1210/jc.2004-2567
10.1530/ERC-14-0465
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Keywords testis
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References 2015082118490611000_226.3.181.40
2015082118490611000_226.3.181.41
2015082118490611000_226.3.181.20
2015082118490611000_226.3.181.42
2015082118490611000_226.3.181.18
2015082118490611000_226.3.181.19
2015082118490611000_226.3.181.14
2015082118490611000_226.3.181.36
2015082118490611000_226.3.181.15
2015082118490611000_226.3.181.37
2015082118490611000_226.3.181.16
2015082118490611000_226.3.181.38
2015082118490611000_226.3.181.17
2015082118490611000_226.3.181.39
2015082118490611000_226.3.181.10
2015082118490611000_226.3.181.32
2015082118490611000_226.3.181.11
2015082118490611000_226.3.181.33
2015082118490611000_226.3.181.12
2015082118490611000_226.3.181.34
2015082118490611000_226.3.181.13
2015082118490611000_226.3.181.35
2015082118490611000_226.3.181.30
2015082118490611000_226.3.181.31
2015082118490611000_226.3.181.9
2015082118490611000_226.3.181.29
2015082118490611000_226.3.181.4
2015082118490611000_226.3.181.25
2015082118490611000_226.3.181.3
2015082118490611000_226.3.181.26
2015082118490611000_226.3.181.2
2015082118490611000_226.3.181.27
2015082118490611000_226.3.181.1
2015082118490611000_226.3.181.28
2015082118490611000_226.3.181.8
2015082118490611000_226.3.181.21
2015082118490611000_226.3.181.43
2015082118490611000_226.3.181.7
2015082118490611000_226.3.181.22
2015082118490611000_226.3.181.44
2015082118490611000_226.3.181.6
2015082118490611000_226.3.181.23
2015082118490611000_226.3.181.5
2015082118490611000_226.3.181.24
References_xml – ident: 2015082118490611000_226.3.181.36
  doi: 10.1073/pnas.0400782101
– ident: 2015082118490611000_226.3.181.2
  doi: 10.1210/me.15.4.654
– ident: 2015082118490611000_226.3.181.15
  doi: 10.1097/00006676-199001000-00005
– ident: 2015082118490611000_226.3.181.16
  doi: 10.1038/nature11405
– ident: 2015082118490611000_226.3.181.32
  doi: 10.1210/er.2012-1076
– ident: 2015082118490611000_226.3.181.7
  doi: 10.1186/1741-7007-6-49
– ident: 2015082118490611000_226.3.181.14
  doi: 10.1016/j.ygeno.2005.04.008
– ident: 2015082118490611000_226.3.181.23
– ident: 2015082118490611000_226.3.181.24
  doi: 10.1210/en.2011-0109
– ident: 2015082118490611000_226.3.181.21
– ident: 2015082118490611000_226.3.181.30
  doi: 10.1093/nar/29.9.e45
– ident: 2015082118490611000_226.3.181.39
  doi: 10.1016/S0021-9258(18)98767-3
– ident: 2015082118490611000_226.3.181.44
  doi: 10.1007/BF02738704
– ident: 2015082118490611000_226.3.181.18
  doi: 10.1210/endo-112-3-951
– ident: 2015082118490611000_226.3.181.41
  doi: 10.1152/ajplung.00360.2012
– ident: 2015082118490611000_226.3.181.4
  doi: 10.1210/me.15.4.668
– ident: 2015082118490611000_226.3.181.9
  doi: 10.1074/jbc.R200021200
– ident: 2015082118490611000_226.3.181.25
  doi: 10.1530/eje.1.01937
– ident: 2015082118490611000_226.3.181.38
  doi: 10.1007/978-3-540-89979-2_3
– ident: 2015082118490611000_226.3.181.10
  doi: 10.1677/joe.0.1820055
– ident: 2015082118490611000_226.3.181.6
  doi: 10.1111/j.1365-2826.2008.01676.x
– ident: 2015082118490611000_226.3.181.3
  doi: 10.1128/MCB.23.14.4882-4891.2003
– ident: 2015082118490611000_226.3.181.43
  doi: 10.1073/pnas.94.20.10862
– ident: 2015082118490611000_226.3.181.12
  doi: 10.1210/er.2013-1087
– ident: 2015082118490611000_226.3.181.34
  doi: 10.1159/000164066
– ident: 2015082118490611000_226.3.181.17
  doi: 10.1210/jc.2013-2743
– ident: 2015082118490611000_226.3.181.22
  doi: 10.1006/geno.1997.5156
– ident: 2015082118490611000_226.3.181.13
  doi: 10.1016/S0378-1119(98)00253-4
– ident: 2015082118490611000_226.3.181.28
– ident: 2015082118490611000_226.3.181.20
  doi: 10.1007/BF00130513
– ident: 2015082118490611000_226.3.181.26
  doi: 10.1210/edrv-3-4-404
– ident: 2015082118490611000_226.3.181.40
  doi: 10.1016/j.freeradbiomed.2003.12.007
– ident: 2015082118490611000_226.3.181.31
  doi: 10.1074/jbc.M807527200
– ident: 2015082118490611000_226.3.181.37
  doi: 10.1038/ng.2453
– ident: 2015082118490611000_226.3.181.42
– ident: 2015082118490611000_226.3.181.33
  doi: 10.1186/1471-2164-10-269
– ident: 2015082118490611000_226.3.181.29
  doi: 10.1210/jc.2012-1616
– ident: 2015082118490611000_226.3.181.5
  doi: 10.1210/en.141.7.2600
– ident: 2015082118490611000_226.3.181.19
  doi: 10.1210/en.132.3.1207
– ident: 2015082118490611000_226.3.181.8
  doi: 10.1055/s-2007-978911
– ident: 2015082118490611000_226.3.181.27
  doi: 10.1038/sj.onc.1208479
– ident: 2015082118490611000_226.3.181.35
  doi: 10.1073/pnas.012025199
– ident: 2015082118490611000_226.3.181.1
  doi: 10.1210/jc.2004-2567
– ident: 2015082118490611000_226.3.181.11
  doi: 10.1530/ERC-14-0465
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Snippet Loss-of-function mutations in the immunoglobulin superfamily member 1 (IGSF1) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism,...
Loss-of-function mutations in the immunoglobulin superfamily member 1 ( IGSF1 ) gene cause an X-linked syndrome of central hypothyroidism, macroorchidism,...
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StartPage 181
SubjectTerms Animals
Brain - metabolism
Female
Gene Expression Regulation, Developmental
Immunoglobulins - genetics
Immunoglobulins - metabolism
Liver - metabolism
Male
Membrane Proteins - genetics
Membrane Proteins - metabolism
Myocardium - metabolism
Organ Specificity
Pancreas - metabolism
Rats
Testis - metabolism
Title Spatial and temporal expression of immunoglobulin superfamily member 1 in the rat
URI http://dx.doi.org/10.1530/JOE-15-0204
https://www.ncbi.nlm.nih.gov/pubmed/26163525
https://www.proquest.com/docview/1706209824
Volume 226
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