Expression Patterns of CREBs in Oocyte Growth and Maturation of Fish

PLoS One. 2015 Dec 23;10(12):e0145182. doi: 10.1371/journal.pone.0145182. eCollection 2015.

Abstract

In fish, oocyte meiotic maturation is regulated by 17α, 20β-dihydroxy-progesterone through cAMP. To study the role of cAMP response element binding protein (CREB) in meiotic maturation, we cloned and characterized the expression pattern of CREBs from two fish models, the Nile tilapia and catfish. In the Nile tilapia three different CREBs were identified where in CREB1 was found in many tissues including gonads with abundant expression in testis. CREB2, few amino acids shorter than CREB1, was expressed in several tissues with abundant expression in ovary. In addition, a 3'UTR variant form, CREB3 was exclusively found in ovary. During natural 14-day ovarian cycle of the Nile tilapia, CREB1 expression was stable throughout vitellogenesis with a sharp decrease on the day of spawning. In contrast, CREB2 remain unchanged throughout the ovarian cycle, however elevated in 11-day full-grown immature ovarian follicle and after hCG-induction. Interestingly, CREB3 expression was induced three folds on the day of spawning as well as during hCG-induced oocyte maturation. Based on the synergistic expression pattern, CREB1 is likely to control oocyte growth, whereas CREB 2 and 3 contribute to oocyte maturation in tilapia and the latter seems to be critical. In catfish, a single form of CREB showed a maximum expression during spawning phase and hCG-induced maturation both in vivo and in vitro augmented CREB expression. These results suggest that spatial and temporal expression of CREBs seems to be important for final oocyte maturation and may also regulate oocyte growth in fish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Catfishes / genetics
  • Catfishes / metabolism*
  • Cloning, Molecular
  • Cyclic AMP Response Element-Binding Protein / genetics
  • Cyclic AMP Response Element-Binding Protein / metabolism*
  • DNA, Complementary / chemistry
  • Female
  • Fish Proteins / genetics
  • Fish Proteins / metabolism*
  • Gene Expression Profiling
  • Male
  • Molecular Sequence Data
  • Oocytes / growth & development
  • Oocytes / metabolism*
  • Phylogeny
  • Sequence Alignment
  • Tilapia / genetics
  • Tilapia / metabolism*
  • Vitellogenesis

Substances

  • Cyclic AMP Response Element-Binding Protein
  • DNA, Complementary
  • Fish Proteins

Grants and funding

Grants-in-aid for Research from CREST (Core Research for Evolutional Science and Technology), JST (Japan Science and Technology Corporation), Research for the Future (JSPS-RFTF 96L00401) and Priority Areas (07283104 and 14042267) from the Ministry of Education, Science, Culture, and Sports, Japan, and Bio Design Program from the Ministry of Agriculture, Forestry and Fisheries, Japan to YN is acknowledged. A Grant-in-aid (SP/SO/AS-49/2003) from the Department of Science and Technology (DST), India, to BS is acknowledged. BS and CCS are the recipients of the Japan Society for the Promotion of Science, which is acknowledged. The authors also thank the support from DST-FIST of the Department of Animal Biology and School of Life Sciences. GS acknowledges junior and senior research fellowships from Council of Scientific and Industrial Research, India. BS is a recipient of TATA innovation fellowship, Department of Biotechnology, Government of India, which is duly acknowledged.