Suppr超能文献

猫中首例38,XX(SRY阳性)性发育障碍病例。

The first case of 38,XX (SRY-positive) disorder of sex development in a cat.

作者信息

Szczerbal Izabela, Stachowiak Monika, Dzimira Stanislaw, Sliwa Krystyna, Switonski Marek

机构信息

Department of Genetics and Animal Breeding, Poznan University of Life Sciences, Poznan, Poland.

Department of Pathology, Wroclaw University of Environmental and Life Sciences, Wroclaw, Poland.

出版信息

Mol Cytogenet. 2015 Mar 26;8:22. doi: 10.1186/s13039-015-0128-5. eCollection 2015.

Abstract

BACKGROUND

SRY-positive XX testicular disorder of sex development (DSD) caused by X;Y translocations was not yet reported in domestic animals. In humans it is rarely diagnosed and a majority of clinical features resemble those which are typical for Klinefelter syndrome (KS). Here we describe the first case of SRY-positive XX DSD in a tortoiseshell cat with a rudimentary penis and a lack of scrotum.

RESULTS

Molecular analysis showed the presence of two Y-linked genes (SRY and ZFY) and a normal sequence of the SRY gene. Application of classical cytogenetic techniques revealed two X chromosomes (38,XX), but further FISH studies with the use of the whole X chromosome painting probe and BAC probes specific to the Yp chromosome facilitated identification of Xp;Yp translocation. The SRY gene was localised at a distal position of Xp. The karyotype of the studied case was described as: 38,XX.ish der(X)t(X;Y)(p22;p12)(SRY+). Moreover, the X inactivation status assessed by a sequential R-banding and FISH with the SRY-specific probe showed a random inactivation of the derivative X(SRY) chromosome.

CONCLUSIONS

Our study showed that among DSD tortoiseshell cats, apart from XXY trisomy and XX/XY chimerism, also SRY-positive XX cases may occur. It is hypothesized that the extremely rare occurrence of this abnormality in domestic animals, when compared with humans, may be associated with a different organisation of the Yp arm in these species.

摘要

背景

X;Y易位导致的SRY阳性XX性发育障碍(DSD)在家畜中尚未见报道。在人类中,这种疾病很少被诊断出来,其大多数临床特征与克兰费尔特综合征(KS)的典型特征相似。在此,我们描述了第一例玳瑁猫SRY阳性XX DSD病例,该猫有一个发育不全的阴茎且无阴囊。

结果

分子分析显示存在两个Y连锁基因(SRY和ZFY),且SRY基因序列正常。经典细胞遗传学技术的应用显示有两条X染色体(38,XX),但使用全X染色体涂染探针和Yp染色体特异性BAC探针进行的进一步荧光原位杂交(FISH)研究有助于鉴定Xp;Yp易位。SRY基因定位于Xp的远端位置。所研究病例的核型描述为:38,XX.ish der(X)t(X;Y)(p22;p12)(SRY+)。此外,通过连续R显带和使用SRY特异性探针的FISH评估的X失活状态显示,衍生的X(SRY)染色体发生随机失活。

结论

我们的研究表明,在DSD玳瑁猫中,除了XXY三体和XX/XY嵌合体之外,也可能出现SRY阳性XX病例。据推测,与人类相比,这种异常在家畜中极其罕见的发生情况可能与这些物种中Yp臂的不同结构有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfea/4382857/28317c7a7694/13039_2015_128_Fig4_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验