<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Biomedical Journal</title>
<title_fa>مجله بیومدیکال ایران</title_fa>
<short_title>IBJ</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ibj.pasteur.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1028-852X</journal_id_issn>
<journal_id_issn_online>2008-823X</journal_id_issn_online>
<journal_id_pii>-</journal_id_pii>
<journal_id_doi>10.61882/ibj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>-</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>-</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1398</year>
	<month>2</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<volume>23</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Identification of Two Novel Mutations in KDM3A 
Regulatory Gene in Iranian Infertile Males</title>
	<subject_fa> Related Fields</subject_fa>
	<subject>Related Fields</subject>
	<content_type_fa>مقاله کامل</content_type_fa>
	<content_type>Full Length/Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;strong&gt;Background:&amp;nbsp;&lt;/strong&gt;&lt;font color=&quot;#0782c1&quot;&gt;&lt;b&gt;&amp;nbsp;&lt;/b&gt;&lt;/font&gt;&lt;em&gt;KDM3A &lt;/em&gt;is a key epigenetic regulator expressed in the testis and is required for packaging and condensation of sperm chromatin. To this point, the association of the &lt;em&gt;KDM3A &lt;/em&gt;gene with infertility has not been studied in human. The aim of this study was to screen any new mutation in &lt;em&gt;KDM3A &lt;/em&gt;gene to explore more details of human male infertility. &lt;strong&gt;Methods: &lt;/strong&gt;In this work, 150 infertile men (oligozoospermia and azoospermia) and 150 normal healthy fathers were studied. &amp;nbsp;Polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP) and sequencing were used to screen any mutation in exons 12, 22, and 24 of &lt;em&gt;KDM3A&lt;/em&gt;. &amp;nbsp;&lt;strong&gt;Results: &lt;/strong&gt;The infertile men showed various SSCP patterns for the exons 12 and 24, but not for exon 22. A transversion point mutation in exon 12 and a single nucleotide deletion in exon 24 were detected using sequencing analysis. The transversion mutation was located in the preceding exon of lysine-specific demethylase1 and Jumonji (Jmj)-C domain and the later one (deletion) in the cupin-like motif of KDM3A protein. Neither Y chromosome microdeletions nor partial azoospermia factor deletion was found in these patients. &lt;strong&gt;Conclusion: &lt;/strong&gt;The mutations found in infertile men&amp;nbsp;with otherwise unexplained severe spermatogenic failure could be considered as the origin of their abnormalities.&amp;nbsp;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>KDM3A, Male infertility, Spermatogenic failure</keyword>
	<start_page>220</start_page>
	<end_page>227</end_page>
	<web_url>http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-1-794&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Zohreh </first_name>
	<middle_name></middle_name>
	<last_name>Hojati</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, P. O. Box 81746-73441,  Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Elaheh </first_name>
	<middle_name></middle_name>
	<last_name>Soleimanpour</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, P. O. Box 81746-73441,  Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Seyed-Morteza</first_name>
	<middle_name></middle_name>
	<last_name> Javadirad</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, P. O. Box 81746-73441,  Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohammad Hossein </first_name>
	<middle_name></middle_name>
	<last_name>Nasr-Esfahani</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid>0000-0003-1983-3435</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Isfahan Fertility and Infertility Center, Isfahan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
