Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia
Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and...
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Veröffentlicht in: | American journal of medical genetics 1997-05, Vol.70 (2), p.134-137 |
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creator | Liou, Jui-Der Ma, Yen-Ying Gibson, Lisa H. Su, Hua Charest, Nancy Lau, Yun-Fai Chris Yang-Feng, Teresa L. |
description | Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and lie within interval 5B of the Y chromosome. PCR and sequence analysis indicated that our patient carries a normal SRY gene. For an additional comparison of the patient's inv(Y) with the father, two other Y chromosome sequences were examined. Molecular studies of this familial inverted Y chromosome showed no differences in the ZFY and TSPY genes between the father and the patient suggesting that the short arm of our patient's inv(Y) is identical to that of the patient's father. Southern analysis using a probe of the DAX‐1 gene indicated that a single copy of DSS (dosage sensitive sex reversal) locus was present in the patient. Our results suggest that the abnormal sexual development in our patient is likely attributable to (an)other mechanism(s) than mutation in the SRY gene and dosage alteration of the DAX‐1 gene. Am. J. Med. Genet. 70:134–137, 1997. © 1997 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1096-8628(19970516)70:2<134::AID-AJMG6>3.0.CO;2-Y |
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FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and lie within interval 5B of the Y chromosome. PCR and sequence analysis indicated that our patient carries a normal SRY gene. For an additional comparison of the patient's inv(Y) with the father, two other Y chromosome sequences were examined. Molecular studies of this familial inverted Y chromosome showed no differences in the ZFY and TSPY genes between the father and the patient suggesting that the short arm of our patient's inv(Y) is identical to that of the patient's father. Southern analysis using a probe of the DAX‐1 gene indicated that a single copy of DSS (dosage sensitive sex reversal) locus was present in the patient. Our results suggest that the abnormal sexual development in our patient is likely attributable to (an)other mechanism(s) than mutation in the SRY gene and dosage alteration of the DAX‐1 gene. Am. J. Med. Genet. 70:134–137, 1997. © 1997 Wiley‐Liss, Inc.</description><identifier>ISSN: 0148-7299</identifier><identifier>EISSN: 1096-8628</identifier><identifier>DOI: 10.1002/(SICI)1096-8628(19970516)70:2<134::AID-AJMG6>3.0.CO;2-Y</identifier><identifier>PMID: 9128931</identifier><identifier>CODEN: AJMGDA</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>ambiguous genitalia ; Biological and medical sciences ; Chromosome aberrations ; Chromosome Inversion ; Disorders of Sex Development ; familial ; Gonadal Dysgenesis, 46,XY - genetics ; Humans ; In Situ Hybridization, Fluorescence ; Infant, Newborn ; inverted Y ; Male ; Medical genetics ; Medical sciences ; Y Chromosome - genetics</subject><ispartof>American journal of medical genetics, 1997-05, Vol.70 (2), p.134-137</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><rights>1997 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4346-e163ceaea1836a5bcbceb419cce1afa453411a57d00979f33a2e934a636b95cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2657685$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9128931$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liou, Jui-Der</creatorcontrib><creatorcontrib>Ma, Yen-Ying</creatorcontrib><creatorcontrib>Gibson, Lisa H.</creatorcontrib><creatorcontrib>Su, Hua</creatorcontrib><creatorcontrib>Charest, Nancy</creatorcontrib><creatorcontrib>Lau, Yun-Fai Chris</creatorcontrib><creatorcontrib>Yang-Feng, Teresa L.</creatorcontrib><title>Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia</title><title>American journal of medical genetics</title><addtitle>Am. J. Med. Genet</addtitle><description>Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and lie within interval 5B of the Y chromosome. PCR and sequence analysis indicated that our patient carries a normal SRY gene. For an additional comparison of the patient's inv(Y) with the father, two other Y chromosome sequences were examined. Molecular studies of this familial inverted Y chromosome showed no differences in the ZFY and TSPY genes between the father and the patient suggesting that the short arm of our patient's inv(Y) is identical to that of the patient's father. Southern analysis using a probe of the DAX‐1 gene indicated that a single copy of DSS (dosage sensitive sex reversal) locus was present in the patient. Our results suggest that the abnormal sexual development in our patient is likely attributable to (an)other mechanism(s) than mutation in the SRY gene and dosage alteration of the DAX‐1 gene. Am. J. Med. Genet. 70:134–137, 1997. © 1997 Wiley‐Liss, Inc.</description><subject>ambiguous genitalia</subject><subject>Biological and medical sciences</subject><subject>Chromosome aberrations</subject><subject>Chromosome Inversion</subject><subject>Disorders of Sex Development</subject><subject>familial</subject><subject>Gonadal Dysgenesis, 46,XY - genetics</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Infant, Newborn</subject><subject>inverted Y</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Y Chromosome - genetics</subject><issn>0148-7299</issn><issn>1096-8628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v00AQhi0EKmnhJyD5gFB7cNgPe-0NCBQZSIMKQSoohMtovFm3C_5Id21Kzvxx1iTkAhKn1c48886reYPgJSVjSgh7eno5z-dnlEgRZYJlp1TKlCRUnKVkwp5THk8m0_mraPr23Uy84GMyzhfPWLS6E4wOM3eDEaFxFqVMyvvBsXNfCaG-wI6CI0lZJjkdBT_zbdde6UZ3RoXYrMO6rbTqK7Sh6_q10S5syxDDEmtTGazCDVpUuums503zXVtn2mZgVqG6tm3durbW4cZq5yFP-NkNdmb43JruOsS6MFd927vQbzUdetEHwb0SK6cf7t-T4NOb1x_z8-hiMZvn04tIxTwWkaaCK40aacYFJoUqlC5iKpXSFEuMEx5Tikm6JkSmsuQcmZY8RsFFIROl-EnwZKe7se1Nr10HtXFKVxU22huCNJMx4ynx4HIHKts6Z3UJG2tqtFugBIZ4AIZ4YDg1DKeGP_FASoCBjwfAxwO_4wEOBPKFr6-88qO9hb6o9fqgu8_D9x_v--gUVqXFRhl3wJhIUpElHvu8w25Npbd_ufuvuX952xW8dLSTNq7TPw7SaL-BSHmawPL9DNiHc_FlmXG45L8AlO7KdQ</recordid><startdate>19970516</startdate><enddate>19970516</enddate><creator>Liou, Jui-Der</creator><creator>Ma, Yen-Ying</creator><creator>Gibson, Lisa H.</creator><creator>Su, Hua</creator><creator>Charest, Nancy</creator><creator>Lau, Yun-Fai Chris</creator><creator>Yang-Feng, Teresa L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</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></search><sort><creationdate>19970516</creationdate><title>Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia</title><author>Liou, Jui-Der ; Ma, Yen-Ying ; Gibson, Lisa H. ; Su, Hua ; Charest, Nancy ; Lau, Yun-Fai Chris ; Yang-Feng, Teresa L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4346-e163ceaea1836a5bcbceb419cce1afa453411a57d00979f33a2e934a636b95cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>ambiguous genitalia</topic><topic>Biological and medical sciences</topic><topic>Chromosome aberrations</topic><topic>Chromosome Inversion</topic><topic>Disorders of Sex Development</topic><topic>familial</topic><topic>Gonadal Dysgenesis, 46,XY - genetics</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Infant, Newborn</topic><topic>inverted Y</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Y Chromosome - genetics</topic><toplevel>online_resources</toplevel><creatorcontrib>Liou, Jui-Der</creatorcontrib><creatorcontrib>Ma, Yen-Ying</creatorcontrib><creatorcontrib>Gibson, Lisa H.</creatorcontrib><creatorcontrib>Su, Hua</creatorcontrib><creatorcontrib>Charest, Nancy</creatorcontrib><creatorcontrib>Lau, Yun-Fai Chris</creatorcontrib><creatorcontrib>Yang-Feng, Teresa L.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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><jtitle>American journal of medical genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liou, Jui-Der</au><au>Ma, Yen-Ying</au><au>Gibson, Lisa H.</au><au>Su, Hua</au><au>Charest, Nancy</au><au>Lau, Yun-Fai Chris</au><au>Yang-Feng, Teresa L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia</atitle><jtitle>American journal of medical genetics</jtitle><addtitle>Am. J. Med. Genet</addtitle><date>1997-05-16</date><risdate>1997</risdate><volume>70</volume><issue>2</issue><spage>134</spage><epage>137</epage><pages>134-137</pages><issn>0148-7299</issn><eissn>1096-8628</eissn><coden>AJMGDA</coden><abstract>Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients and the father's Ys appear to be the same and lie within interval 5B of the Y chromosome. PCR and sequence analysis indicated that our patient carries a normal SRY gene. For an additional comparison of the patient's inv(Y) with the father, two other Y chromosome sequences were examined. Molecular studies of this familial inverted Y chromosome showed no differences in the ZFY and TSPY genes between the father and the patient suggesting that the short arm of our patient's inv(Y) is identical to that of the patient's father. Southern analysis using a probe of the DAX‐1 gene indicated that a single copy of DSS (dosage sensitive sex reversal) locus was present in the patient. Our results suggest that the abnormal sexual development in our patient is likely attributable to (an)other mechanism(s) than mutation in the SRY gene and dosage alteration of the DAX‐1 gene. Am. J. Med. Genet. 70:134–137, 1997. © 1997 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9128931</pmid><doi>10.1002/(SICI)1096-8628(19970516)70:2<134::AID-AJMG6>3.0.CO;2-Y</doi><tpages>4</tpages></addata></record> |
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subjects | ambiguous genitalia Biological and medical sciences Chromosome aberrations Chromosome Inversion Disorders of Sex Development familial Gonadal Dysgenesis, 46,XY - genetics Humans In Situ Hybridization, Fluorescence Infant, Newborn inverted Y Male Medical genetics Medical sciences Y Chromosome - genetics |
title | Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia |
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