4.5 Article

Secretagogin in the brain and pituitary of the catfish, Clarias batrachus: Molecular characterization and regulation by insulin

期刊

JOURNAL OF COMPARATIVE NEUROLOGY
卷 530, 期 11, 页码 1743-1772

出版社

WILEY
DOI: 10.1002/cne.25311

关键词

brain; Ca2+-binding protein; insulin; pituitary; preoptic area; secretagogin; teleost

资金

  1. NISER, Bhubaneswar, Department of Atomic Energy (DAE), Government of India
  2. Science and Engineering Research Board (SERB)
  3. Department of Science and Technology (DST), Government of India [SR/SO/AS-83/2010]

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This study investigated the expression and distribution of scgn gene in the brain and pituitary of a teleost, Clarias batrachus. The study found that scgn was widely expressed in the brain and pituitary, with higher expression in the telencephalon. Immunohistochemical analysis revealed scgn expression in neurons in the brain and certain areas of the pituitary. Insulin was found to regulate scgn expression in the telencephalon. These results suggest that scgn may play an important role in the regulation of olfactory, neuroendocrine system, and energy balance functions in C. batrachus.
Secretagogin (scgn), is a novel hexa EF-hand, phylogenetically conserved calcium-binding protein. It serves as Ca2+ sensor and participates in Ca2+-signaling and neuroendocrine regulation in mammals. However, its relevance in the brain of non-mammalian vertebrates has largely remained unexplored. To address this issue, we studied the cDNA encoding scgn, scgn mRNA expression, and distribution of scgn-equipped elements in the brain and pituitary of a teleost, Clarias batrachus (cb). The cbscgn cDNA consists of three transcripts (T) variants: T1 (2185 bp), T2 (2151 bp) and T3 (2060 bp). While 816 bp ORF in T1 and T2 encodes highly conserved six EF-hand 272 aa protein fully capable of Ca2+-binding, 726-bp ORF in T3 encodes 242 aa protein. The T1 showed >90% and >70% identity with scgn of catfishes, and other teleosts and mammals, respectively. The T1-mRNA was widely expressed in the brain and pituitary, while the expression of T3 was restricted to the telencephalon. Application of the anti-scgn antiserum revealed a similar to 32 kDa scgn-immunoreactive (scgn-i) band (known molecular weight of scgn) in the forebrain tissue, and immunohistochemically labeled neurons in the olfactory epithelium and bulb, telencephalon, preoptic area, hypothalamus, thalamus, and hindbrain. In the pituitary, scgn-i cells were seen in the pars distalis and intermedia. Insulin is reported to regulate scgn mRNA in the mammalian hippocampus, and feeding-related neuropeptides in the telencephalon of teleost. Intracranial injection of insulin significantly increased T1-mRNA expression and scgn-immunoreactivity in the telencephalon. We suggest that scgn may be an important player in the regulation of olfactory, neuroendocrine system, and energy balance functions in C. batrachus.

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