Ablation of the scaffold protein JLP causes reduced fertility in male mice

Asuka Iwanaga, Guangmin Wang, Davaakhuu Gantulga, Tokiharu Sato, Tuvshintugs Baljinnyam, Keiko Shimizu, Ken Takumi, Motoharu Hayashi, Takuya Akashi, Hideki Fuse, Kazushi Sugihara, Masahide Asano, Katsuji Yoshioka

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

The specific and efficient activation of mitogen-activated protein kinase (MAPK) signaling modules is mediated, at least in part, by scaffold proteins. c-Jun NH2-terminal kinase (JNK)-associated leucine zipper protein (JLP) was identified as a scaffold protein for JNK and p38 MAPK signaling modules. JLP is expressed nearly ubiquitously and is involved in intracellular signaling pathways, such as the Gα13 and Cdo-mediated pathway, in vitro. To date, however, JLP expression has not been analyzed in detail, nor are its physiological functions well understood. Here we investigated the expression of JLP in the mouse testis during development. Of the tissues examined, JLP was strongest in the testis, with the most intense staining in the elongated spermatids. Since the anti-JLP antibody used in this study can recognize both JLP and sperm-associated antigen 9 (SPAG9), a splice variant of JLP that has been studied extensively in primates, we also examined its expression in macaque testis samples. Our results indicated that in mouse and primate testis, the isoform expressed at the highest level was JLP, not SPAG9. We also investigated the function of JLP by disrupting the Jlp gene in mice, and found that the male homozygotes were subfertile. Taken together, these observations may suggest that JLP plays an important role in testis during development, especially in the production of functionally normal spermatozoa.

Original languageEnglish (US)
Pages (from-to)1045-1058
Number of pages14
JournalTransgenic Research
Volume17
Issue number6
DOIs
StatePublished - Dec 2008
Externally publishedYes

Fingerprint

scaffolding proteins
male fertility
Fertility
Testis
testes
mitogen-activated protein kinase
mice
Spermatozoa
JNK Mitogen-Activated Protein Kinases
spermatozoa
Proteins
Primates
antigens
Antigens
Leucine Zippers
leucine zipper
Spermatids
spermatids
Homozygote
Macaca

Keywords

  • JLP
  • Knockout mouse
  • MAP kinase
  • Scaffold protein
  • Signal transduction
  • SPAG9

ASJC Scopus subject areas

  • Biotechnology
  • Animal Science and Zoology
  • Agronomy and Crop Science
  • Genetics

Cite this

Iwanaga, A., Wang, G., Gantulga, D., Sato, T., Baljinnyam, T., Shimizu, K., ... Yoshioka, K. (2008). Ablation of the scaffold protein JLP causes reduced fertility in male mice. Transgenic Research, 17(6), 1045-1058. https://doi.org/10.1007/s11248-008-9191-6

Ablation of the scaffold protein JLP causes reduced fertility in male mice. / Iwanaga, Asuka; Wang, Guangmin; Gantulga, Davaakhuu; Sato, Tokiharu; Baljinnyam, Tuvshintugs; Shimizu, Keiko; Takumi, Ken; Hayashi, Motoharu; Akashi, Takuya; Fuse, Hideki; Sugihara, Kazushi; Asano, Masahide; Yoshioka, Katsuji.

In: Transgenic Research, Vol. 17, No. 6, 12.2008, p. 1045-1058.

Research output: Contribution to journalArticle

Iwanaga, A, Wang, G, Gantulga, D, Sato, T, Baljinnyam, T, Shimizu, K, Takumi, K, Hayashi, M, Akashi, T, Fuse, H, Sugihara, K, Asano, M & Yoshioka, K 2008, 'Ablation of the scaffold protein JLP causes reduced fertility in male mice', Transgenic Research, vol. 17, no. 6, pp. 1045-1058. https://doi.org/10.1007/s11248-008-9191-6
Iwanaga A, Wang G, Gantulga D, Sato T, Baljinnyam T, Shimizu K et al. Ablation of the scaffold protein JLP causes reduced fertility in male mice. Transgenic Research. 2008 Dec;17(6):1045-1058. https://doi.org/10.1007/s11248-008-9191-6
Iwanaga, Asuka ; Wang, Guangmin ; Gantulga, Davaakhuu ; Sato, Tokiharu ; Baljinnyam, Tuvshintugs ; Shimizu, Keiko ; Takumi, Ken ; Hayashi, Motoharu ; Akashi, Takuya ; Fuse, Hideki ; Sugihara, Kazushi ; Asano, Masahide ; Yoshioka, Katsuji. / Ablation of the scaffold protein JLP causes reduced fertility in male mice. In: Transgenic Research. 2008 ; Vol. 17, No. 6. pp. 1045-1058.
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