Mamld1 deficiency significantly reduces mRNA expression levels of multiple genes expressed in mouse fetal leydig cells but permits normal genital and reproductive development

Mami Miyado, Michiko Nakamura, Kenji Miyado, Ken Ichirou Morohashi, Shinichiro Sano, Eiko Nagata, Maki Fukami, Tsutomu Ogata

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Although mastermind-like domain containing 1 (MAMLD1) (CXORF6) on human chromosome Xq28 has been shown to be a causative gene for 46,XY disorders of sex development with hypospadias, the biological function of MAMLD1/Mamld1 remains to be elucidated. In this study, we first showed gradual and steady increase of testicular Mamld1 mRNA expression levels in wild-type male mice from 12.5 to 18.5 d postcoitum. We then generated Mamld1 knockout (KO) male mice and revealed mildly but significantly reduced testicular mRNA levels (65-80%) of genes exclusively expressed in Leydig cells (Star, Cyp11a1, Cyp17a1, Hsd3b1, and Insl3) as well as grossly normal testicular mRNA levels of genes expressed in other cell types or in Leydig and other cell types. However, no demonstrable abnormality was identified for cytochrome P450 17A1 and 3β-hydroxysteroid dehydrogenase (HSD3B) protein expression levels, appearance of external and internal genitalia, anogenital distance, testis weight, Leydig cell number, intratesticular testosterone and other steroid metabolite concentrations, histological findings, in situ hybridization findings for sonic hedgehog (the key molecule for genital tubercle development), and immunohistochemical findings for anti-Müllerian hormone (Sertoli cell marker), HSD3B (Leydig cell marker), and DEAD (Asp-Glu-Ala-Asp) box polypeptide 4 (germ cell marker) in the KO male mice. Fertility was also normal. These findings imply that Mamld1 deficiency significantly reduces mRNA expression levels of multiple genes expressed in mouse fetal Leydig cells but permits normal genital and reproductive development. The contrastive phenotypic findings between Mamld1 KO male mice and MAMLD1 mutation positive patients would primarily be ascribed to species difference in the fetal sex development.

Original languageEnglish
Pages (from-to)6033-6040
Number of pages8
JournalEndocrinology
Volume153
Issue number12
DOIs
Publication statusPublished - Dec 1 2012

Fingerprint

Leydig Cells
Messenger RNA
Knockout Mice
Genes
3-Hydroxysteroid Dehydrogenases
XY Disorders of Sex Development 46
Hypospadias
Sexual Development
Genitalia
Hedgehogs
Sertoli Cells
Human Chromosomes
Fetal Development
Germ Cells
Cytochrome P-450 Enzyme System
In Situ Hybridization
Fertility
Testosterone
Testis
Cell Count

All Science Journal Classification (ASJC) codes

  • Endocrinology

Cite this

Mamld1 deficiency significantly reduces mRNA expression levels of multiple genes expressed in mouse fetal leydig cells but permits normal genital and reproductive development. / Miyado, Mami; Nakamura, Michiko; Miyado, Kenji; Morohashi, Ken Ichirou; Sano, Shinichiro; Nagata, Eiko; Fukami, Maki; Ogata, Tsutomu.

In: Endocrinology, Vol. 153, No. 12, 01.12.2012, p. 6033-6040.

Research output: Contribution to journalArticle

Miyado, Mami ; Nakamura, Michiko ; Miyado, Kenji ; Morohashi, Ken Ichirou ; Sano, Shinichiro ; Nagata, Eiko ; Fukami, Maki ; Ogata, Tsutomu. / Mamld1 deficiency significantly reduces mRNA expression levels of multiple genes expressed in mouse fetal leydig cells but permits normal genital and reproductive development. In: Endocrinology. 2012 ; Vol. 153, No. 12. pp. 6033-6040.
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