SEPT12/SPAG4/LAMINB1 complexes are required for maintaining the integrity of the nuclear envelope in postmeiotic male germ cells

PLoS One. 2015 Mar 16;10(3):e0120722. doi: 10.1371/journal.pone.0120722. eCollection 2015.

Abstract

Male infertility affects approximately 50% of all infertile couples. The male-related causes of intracytoplasmic sperm injection failure include the absence of sperm, immotile or immature sperm, and sperm with structural defects such as those caused by premature chromosomal condensation and DNA damage. Our previous studies based on a knockout mice model indicated that SEPT12 proteins are critical for the terminal morphological formation of sperm. SEPT12 mutations in men result in teratozospermia and oligozospermia. In addition, the spermatozoa exhibit morphological defects of the head and tail, premature chromosomal condensation, and nuclear damage. However, the molecular functions of SEPT12 during spermatogenesis remain unclear. To determine the molecular functions of SEPT12, we applied a yeast 2-hybrid system to identify SEPT12 interactors. Seven proteins that interact with SEPT12 were identified: SEPT family proteins (SEPT4 and SEPT6), nuclear or nuclear membrane proteins (protamine 2, sperm-associated antigen 4, and NDC1 transmembrane nucleoproine), and sperm-related structural proteins (pericentriolar material 1 and obscurin-like 1). Sperm-associated antigen 4 (SPAG4; also known as SUN4) belongs to the SUN family of proteins and acts as a linker protein between nucleoskeleton and cytoskeleton proteins and localizes in the nuclear membrane. We determined that SEPT12 interacts with SPAG4 in a male germ cell line through coimmunoprecipitation. During human spermiogenesis, SEPT12 is colocalized with SPAG4 near the nuclear periphery in round spermatids and in the centrosome region in elongating spermatids. Furthermore, we observed that SEPT12/SPAG4/LAMINB1 formed complexes and were coexpressed in the nuclear periphery of round spermatids. In addition, mutated SEPT12, which was screened from an infertile man, affected the integration of these nuclear envelope complexes through coimmunoprecipitation. This was the first study that suggested that SEPT proteins link to the SUN/LAMIN complexes during the formation of nuclear envelopes and are involved in the development of postmeiotic germ cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / metabolism*
  • Humans
  • Lamin Type B / metabolism*
  • Male
  • Meiosis
  • Nuclear Envelope / metabolism*
  • Protein Binding
  • Septins / metabolism*
  • Spermatogenesis
  • Spermatozoa / cytology
  • Spermatozoa / metabolism*

Substances

  • Carrier Proteins
  • Lamin Type B
  • SPAG4 protein, human
  • SEPTIN12 protein, human
  • Septins

Grants and funding

This study was supported by grants from the Ministry of Science and Technology of the Republic of China (YHL: NSC 101-2320-B-030-012-MY2, NSC 102-2320-B-030 -006 -MY3 and MOST 103-2314-B-030-002-), Shin-Kong Wu Ho-Su Memorial Hospital (YHL: 101-SKH-FJU-06), and Cathay General Hospital (YHL: 102-CGH-FJU-03). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.