Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX

Abstract Objectives: The etiology of gonadal dysgenesis and ovotesticular syndrome is unknown in a majority of cases. The aim of the study was to perform cytogenetic and molecular characterization of a group of patients with ovotesticular syndrome and complete gonadal dysgenesis from peripheral blood and gonadal tissue samples. Materials and methods: A total of 6 patients were included, 3 with diagnosis of 46,XX ovotesticular syndrome, one diagnosed with 46,XY ovotesticular syndrome; one with suspected 46,XX gonadal dysgenesis, and one with 46,XY complete gonadal dysgenesis. Results: All patients were evaluated with karyotype, fluorescent in situ hybridization (FISH) for SRY, multiplex ligation-dependent probe amplification (MLPA) and comparative genomic hybridization (aCGH) on peripheral blood samples. In cases with available gonadal tissue, the levels of genetic expression of SOX3, SRY, and SOX9 were determined through real-time PCR and immunofluorescence. Rearrangements involving SRY gene were ruled out. No deletions/duplications or copy-number variations (CNV) were detected as the etiology for sexual development disorder in any of the patients studied. In a case of 46,XX ovotesticular syndrome, the gonadal karyotype was different from the karyotype in peripheral blood. Aberrant expression of SOX3 and SOX9 in gonadal tissue of a case with 46,XX ovotesticular syndrome was observed. Conclusions: Lower levels of expression of SRY and SOX9 compared to the levels in human cellular lines of embryonic testicle and Sertoli were documented in the gonadal tissue of a case with 46,XY ovotesticular syndrome. Cytogenetic and molecular studies of the gonads as a complement to peripheral blood study have the potential to enrich the understanding of sexual development disorders in patients who are XX or XY in peripheral blood.

Saved in:
Bibliographic Details
Main Authors: Manotas,María Carolina, García-Acero,Mary, González,Daniel, Bernal,Camila, Guerra,Mariana, Moreno-Niño,Olga, Suárez,Fernando, Céspedes,Camila, Forero,Catalina, Pérez,Jaime, Rojas,Adriana
Format: Digital revista
Language:English
Published: Sociedad Mexicana de Urología 2021
Online Access:http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S2007-40852021000400001
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S2007-40852021000400001
record_format ojs
spelling oai:scielo:S2007-408520210004000012023-04-19Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XXManotas,María CarolinaGarcía-Acero,MaryGonzález,DanielBernal,CamilaGuerra,MarianaMoreno-Niño,OlgaSuárez,FernandoCéspedes,CamilaForero,CatalinaPérez,JaimeRojas,Adriana gonadal dysgenesis ovotesticular syndrome FISH MLPA aCGH SRY Abstract Objectives: The etiology of gonadal dysgenesis and ovotesticular syndrome is unknown in a majority of cases. The aim of the study was to perform cytogenetic and molecular characterization of a group of patients with ovotesticular syndrome and complete gonadal dysgenesis from peripheral blood and gonadal tissue samples. Materials and methods: A total of 6 patients were included, 3 with diagnosis of 46,XX ovotesticular syndrome, one diagnosed with 46,XY ovotesticular syndrome; one with suspected 46,XX gonadal dysgenesis, and one with 46,XY complete gonadal dysgenesis. Results: All patients were evaluated with karyotype, fluorescent in situ hybridization (FISH) for SRY, multiplex ligation-dependent probe amplification (MLPA) and comparative genomic hybridization (aCGH) on peripheral blood samples. In cases with available gonadal tissue, the levels of genetic expression of SOX3, SRY, and SOX9 were determined through real-time PCR and immunofluorescence. Rearrangements involving SRY gene were ruled out. No deletions/duplications or copy-number variations (CNV) were detected as the etiology for sexual development disorder in any of the patients studied. In a case of 46,XX ovotesticular syndrome, the gonadal karyotype was different from the karyotype in peripheral blood. Aberrant expression of SOX3 and SOX9 in gonadal tissue of a case with 46,XX ovotesticular syndrome was observed. Conclusions: Lower levels of expression of SRY and SOX9 compared to the levels in human cellular lines of embryonic testicle and Sertoli were documented in the gonadal tissue of a case with 46,XY ovotesticular syndrome. Cytogenetic and molecular studies of the gonads as a complement to peripheral blood study have the potential to enrich the understanding of sexual development disorders in patients who are XX or XY in peripheral blood.info:eu-repo/semantics/openAccessSociedad Mexicana de UrologíaRevista mexicana de urología v.81 n.4 20212021-08-01info:eu-repo/semantics/articletext/htmlhttp://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S2007-40852021000400001en10.48193/rmu.v81i4.779
institution SCIELO
collection OJS
country México
countrycode MX
component Revista
access En linea
databasecode rev-scielo-mx
tag revista
region America del Norte
libraryname SciELO
language English
format Digital
author Manotas,María Carolina
García-Acero,Mary
González,Daniel
Bernal,Camila
Guerra,Mariana
Moreno-Niño,Olga
Suárez,Fernando
Céspedes,Camila
Forero,Catalina
Pérez,Jaime
Rojas,Adriana
spellingShingle Manotas,María Carolina
García-Acero,Mary
González,Daniel
Bernal,Camila
Guerra,Mariana
Moreno-Niño,Olga
Suárez,Fernando
Céspedes,Camila
Forero,Catalina
Pérez,Jaime
Rojas,Adriana
Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX
author_facet Manotas,María Carolina
García-Acero,Mary
González,Daniel
Bernal,Camila
Guerra,Mariana
Moreno-Niño,Olga
Suárez,Fernando
Céspedes,Camila
Forero,Catalina
Pérez,Jaime
Rojas,Adriana
author_sort Manotas,María Carolina
title Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX
title_short Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX
title_full Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX
title_fullStr Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX
title_full_unstemmed Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX
title_sort cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,xy and 46,xx
description Abstract Objectives: The etiology of gonadal dysgenesis and ovotesticular syndrome is unknown in a majority of cases. The aim of the study was to perform cytogenetic and molecular characterization of a group of patients with ovotesticular syndrome and complete gonadal dysgenesis from peripheral blood and gonadal tissue samples. Materials and methods: A total of 6 patients were included, 3 with diagnosis of 46,XX ovotesticular syndrome, one diagnosed with 46,XY ovotesticular syndrome; one with suspected 46,XX gonadal dysgenesis, and one with 46,XY complete gonadal dysgenesis. Results: All patients were evaluated with karyotype, fluorescent in situ hybridization (FISH) for SRY, multiplex ligation-dependent probe amplification (MLPA) and comparative genomic hybridization (aCGH) on peripheral blood samples. In cases with available gonadal tissue, the levels of genetic expression of SOX3, SRY, and SOX9 were determined through real-time PCR and immunofluorescence. Rearrangements involving SRY gene were ruled out. No deletions/duplications or copy-number variations (CNV) were detected as the etiology for sexual development disorder in any of the patients studied. In a case of 46,XX ovotesticular syndrome, the gonadal karyotype was different from the karyotype in peripheral blood. Aberrant expression of SOX3 and SOX9 in gonadal tissue of a case with 46,XX ovotesticular syndrome was observed. Conclusions: Lower levels of expression of SRY and SOX9 compared to the levels in human cellular lines of embryonic testicle and Sertoli were documented in the gonadal tissue of a case with 46,XY ovotesticular syndrome. Cytogenetic and molecular studies of the gonads as a complement to peripheral blood study have the potential to enrich the understanding of sexual development disorders in patients who are XX or XY in peripheral blood.
publisher Sociedad Mexicana de Urología
publishDate 2021
url http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S2007-40852021000400001
work_keys_str_mv AT manotasmariacarolina cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT garciaaceromary cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT gonzalezdaniel cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT bernalcamila cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT guerramariana cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT morenoninoolga cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT suarezfernando cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT cespedescamila cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT forerocatalina cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT perezjaime cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
AT rojasadriana cytogeneticandmolecularcharacterizationingonadaltissueofpatientswithovotesticularsyndromeandgonadaldysgenesis46xyand46xx
_version_ 1764986553227018240