DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease
DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary...
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Veröffentlicht in: | Baillière's best practice & research. Clinical endocrinology & metabolism 2015-08, Vol.29 (4), p.607-619 |
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description | DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people. |
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Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people.</description><identifier>ISSN: 1521-690X</identifier><identifier>EISSN: 1878-1594</identifier><identifier>DOI: 10.1016/j.beem.2015.07.004</identifier><identifier>PMID: 26303087</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>46,XY disorders of sex development ; Addison disease ; Adrenal Insufficiency - genetics ; Adrenal Insufficiency - metabolism ; Adrenal Insufficiency - pathology ; DAX-1 ; DAX-1 Orphan Nuclear Receptor - genetics ; DAX-1 Orphan Nuclear Receptor - metabolism ; Endocrinology & Metabolism ; Genetic Diseases, X-Linked - genetics ; Genetic Diseases, X-Linked - metabolism ; Genetic Diseases, X-Linked - pathology ; Humans ; Hypoadrenocorticism, Familial ; hypogonadotropic hypogonadism ; hypospadias ; infertility ; Male ; Mutation ; Phenotype ; primary adrenal insufficiency ; primary ovarian insufficiency ; SF-1 ; Steroidogenic Factor 1 - genetics ; Steroidogenic Factor 1 - metabolism ; X-linked adrenal hypoplasia congenita</subject><ispartof>Baillière's best practice & research. Clinical endocrinology & metabolism, 2015-08, Vol.29 (4), p.607-619</ispartof><rights>The Authors</rights><rights>2015 The Authors</rights><rights>Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-efe73350d897589299c2c22c34c9fee2217a7de8727b4735bfe05e9d6d6461a23</citedby><cites>FETCH-LOGICAL-c510t-efe73350d897589299c2c22c34c9fee2217a7de8727b4735bfe05e9d6d6461a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.beem.2015.07.004$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26303087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suntharalingham, Jenifer P., BSc</creatorcontrib><creatorcontrib>Buonocore, Federica, PhD</creatorcontrib><creatorcontrib>Duncan, Andrew J., PhD</creatorcontrib><creatorcontrib>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creatorcontrib><title>DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease</title><title>Baillière's best practice & research. Clinical endocrinology & metabolism</title><addtitle>Best Pract Res Clin Endocrinol Metab</addtitle><description>DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people.</description><subject>46,XY disorders of sex development</subject><subject>Addison disease</subject><subject>Adrenal Insufficiency - genetics</subject><subject>Adrenal Insufficiency - metabolism</subject><subject>Adrenal Insufficiency - pathology</subject><subject>DAX-1</subject><subject>DAX-1 Orphan Nuclear Receptor - genetics</subject><subject>DAX-1 Orphan Nuclear Receptor - metabolism</subject><subject>Endocrinology & Metabolism</subject><subject>Genetic Diseases, X-Linked - genetics</subject><subject>Genetic Diseases, X-Linked - metabolism</subject><subject>Genetic Diseases, X-Linked - pathology</subject><subject>Humans</subject><subject>Hypoadrenocorticism, Familial</subject><subject>hypogonadotropic hypogonadism</subject><subject>hypospadias</subject><subject>infertility</subject><subject>Male</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>primary adrenal insufficiency</subject><subject>primary ovarian insufficiency</subject><subject>SF-1</subject><subject>Steroidogenic Factor 1 - genetics</subject><subject>Steroidogenic Factor 1 - metabolism</subject><subject>X-linked adrenal hypoplasia congenita</subject><issn>1521-690X</issn><issn>1878-1594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9ktFr1TAUxos43Jz-Az5IHyfYek7SNC3I4DrdJowJm8LeQm5yuuXaNlvSDvbfm3LnUB98SiDf9-Xw_U6WvUEoEbD-sCnXREPJAEUJsgSonmV72MimQNFWz9NdMCzqFq52s5cxbgAAOeCLbJfVHDg0ci87-by6KjA_OL-AT_gu16PN40TBO-uvaXQm77SZfFgkl8cFvs_PL8QqCd2Y38yDHnPrIulIr7KdTveRXj-e-9mP4y_fj06Ls28nX49WZ4URCFNBHUnOBdimlaJpWdsaZhgzvDJtR8QYSi0tNZLJdSW5WHcEglpb27qqUTO-nx1uc2_n9UDW0DgF3avb4AYdHpTXTv39Mrobde3vlUidyEqkgIPHgODvZoqTGlw01Pd6JD9HhRKkEFUDdZKyrdQEH2Og7ukbBLUQUBu1EFALAQVSJQLJ9PbPAZ8svytPgo9bAaWa7h0FFY2j0ZB1gcykrHf_zz_8x256l0Dp_ic9UNz4OYwJgEIVmQJ1uezAsgIoEn6JDf8FxRmoXA</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Suntharalingham, Jenifer P., BSc</creator><creator>Buonocore, Federica, PhD</creator><creator>Duncan, Andrew J., PhD</creator><creator>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150801</creationdate><title>DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease</title><author>Suntharalingham, Jenifer P., BSc ; Buonocore, Federica, PhD ; Duncan, Andrew J., PhD ; Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-efe73350d897589299c2c22c34c9fee2217a7de8727b4735bfe05e9d6d6461a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>46,XY disorders of sex development</topic><topic>Addison disease</topic><topic>Adrenal Insufficiency - genetics</topic><topic>Adrenal Insufficiency - metabolism</topic><topic>Adrenal Insufficiency - pathology</topic><topic>DAX-1</topic><topic>DAX-1 Orphan Nuclear Receptor - genetics</topic><topic>DAX-1 Orphan Nuclear Receptor - metabolism</topic><topic>Endocrinology & Metabolism</topic><topic>Genetic Diseases, X-Linked - genetics</topic><topic>Genetic Diseases, X-Linked - metabolism</topic><topic>Genetic Diseases, X-Linked - pathology</topic><topic>Humans</topic><topic>Hypoadrenocorticism, Familial</topic><topic>hypogonadotropic hypogonadism</topic><topic>hypospadias</topic><topic>infertility</topic><topic>Male</topic><topic>Mutation</topic><topic>Phenotype</topic><topic>primary adrenal insufficiency</topic><topic>primary ovarian insufficiency</topic><topic>SF-1</topic><topic>Steroidogenic Factor 1 - genetics</topic><topic>Steroidogenic Factor 1 - metabolism</topic><topic>X-linked adrenal hypoplasia congenita</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suntharalingham, Jenifer P., BSc</creatorcontrib><creatorcontrib>Buonocore, Federica, PhD</creatorcontrib><creatorcontrib>Duncan, Andrew J., PhD</creatorcontrib><creatorcontrib>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Baillière's best practice & research. Clinical endocrinology & metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suntharalingham, Jenifer P., BSc</au><au>Buonocore, Federica, PhD</au><au>Duncan, Andrew J., PhD</au><au>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease</atitle><jtitle>Baillière's best practice & research. Clinical endocrinology & metabolism</jtitle><addtitle>Best Pract Res Clin Endocrinol Metab</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>29</volume><issue>4</issue><spage>607</spage><epage>619</epage><pages>607-619</pages><issn>1521-690X</issn><eissn>1878-1594</eissn><abstract>DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>26303087</pmid><doi>10.1016/j.beem.2015.07.004</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 46,XY disorders of sex development Addison disease Adrenal Insufficiency - genetics Adrenal Insufficiency - metabolism Adrenal Insufficiency - pathology DAX-1 DAX-1 Orphan Nuclear Receptor - genetics DAX-1 Orphan Nuclear Receptor - metabolism Endocrinology & Metabolism Genetic Diseases, X-Linked - genetics Genetic Diseases, X-Linked - metabolism Genetic Diseases, X-Linked - pathology Humans Hypoadrenocorticism, Familial hypogonadotropic hypogonadism hypospadias infertility Male Mutation Phenotype primary adrenal insufficiency primary ovarian insufficiency SF-1 Steroidogenic Factor 1 - genetics Steroidogenic Factor 1 - metabolism X-linked adrenal hypoplasia congenita |
title | DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease |
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