Nehareeka Dan, Harsh Shah, Himadri Bhatt, Rahul Ladumor, Ankita Salunke, A. V. Ramachandran, Parth Pandya
{"title":"解码鲤鱼青春期开始时光周期线索在传递吻肽-褪黑激素回路中的作用","authors":"Nehareeka Dan, Harsh Shah, Himadri Bhatt, Rahul Ladumor, Ankita Salunke, A. V. Ramachandran, Parth Pandya","doi":"10.1002/mrd.23744","DOIUrl":null,"url":null,"abstract":"<p>This study unravels the intricate interplay between photoperiod, melatonin, and kisspeptin to orchestrate the pubertal onset of Common carp. Female fingerlings exposed to long days (LD) exhibited a hormonal crescendo, with upregulated hypothalamic-pituitary-ovarian (HPO) axis genes (<i>kiss1</i>, <i>kiss1r</i>, <i>kiss2</i>, <i>gnrh2</i>, <i>gnrh3</i>) and their downstream targets (<i>lhr</i>, <i>fshr</i>, <i>ar1</i>, <i>esr1</i>). However, the expression of the melatonin receptor (<i>mtnr1a</i>) diminished in LD, suggesting a potential inhibitory role. This hormonal symphony was further amplified by increased activity of key transcriptional regulators (<i>gata1</i>, <i>gata2</i>, <i>cdx1</i>, <i>sp1</i>, <i>n-myc</i>, <i>hoxc8</i>, <i>plc</i>, <i>tac3</i>, <i>tacr3</i>) and decreased expression of delayed puberty genes (<i>mkrn1</i>, <i>dlk1</i>). In contrast, short days (SD) muted this hormonal chorus, with decreased <i>gnrh</i> gene and regulator expression, elevated <i>mtnr1a</i>, and suppressed gonadal development. In in-vitro, estradiol mimicked the LD effect, boosting <i>gnrh</i> and regulator genes while dampening <i>mtnr1a</i> and melatonin-responsive genes. Conversely, melatonin acted as a conductor, downregulating <i>gnrh</i> and regulator genes and amplifying <i>mtnr1a</i>. Our findings illuminate the crucial roles of melatonin and kisspeptin as opposing forces in regulating pubertal timing. LD-induced melatonin suppression allows the kisspeptin symphony to flourish, triggering GnRH release and, ultimately, gonadal maturation. This delicate dance between photoperiod, melatonin, and kisspeptin orchestrates common carp's transition from juvenile to reproductive life.</p>","PeriodicalId":18856,"journal":{"name":"Molecular Reproduction and Development","volume":"91 5","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2024-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Decoding the effect of photoperiodic cues in transducing kisspeptin-melatonin circuit during the pubertal onset in common carp\",\"authors\":\"Nehareeka Dan, Harsh Shah, Himadri Bhatt, Rahul Ladumor, Ankita Salunke, A. V. Ramachandran, Parth Pandya\",\"doi\":\"10.1002/mrd.23744\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This study unravels the intricate interplay between photoperiod, melatonin, and kisspeptin to orchestrate the pubertal onset of Common carp. Female fingerlings exposed to long days (LD) exhibited a hormonal crescendo, with upregulated hypothalamic-pituitary-ovarian (HPO) axis genes (<i>kiss1</i>, <i>kiss1r</i>, <i>kiss2</i>, <i>gnrh2</i>, <i>gnrh3</i>) and their downstream targets (<i>lhr</i>, <i>fshr</i>, <i>ar1</i>, <i>esr1</i>). However, the expression of the melatonin receptor (<i>mtnr1a</i>) diminished in LD, suggesting a potential inhibitory role. This hormonal symphony was further amplified by increased activity of key transcriptional regulators (<i>gata1</i>, <i>gata2</i>, <i>cdx1</i>, <i>sp1</i>, <i>n-myc</i>, <i>hoxc8</i>, <i>plc</i>, <i>tac3</i>, <i>tacr3</i>) and decreased expression of delayed puberty genes (<i>mkrn1</i>, <i>dlk1</i>). In contrast, short days (SD) muted this hormonal chorus, with decreased <i>gnrh</i> gene and regulator expression, elevated <i>mtnr1a</i>, and suppressed gonadal development. In in-vitro, estradiol mimicked the LD effect, boosting <i>gnrh</i> and regulator genes while dampening <i>mtnr1a</i> and melatonin-responsive genes. Conversely, melatonin acted as a conductor, downregulating <i>gnrh</i> and regulator genes and amplifying <i>mtnr1a</i>. Our findings illuminate the crucial roles of melatonin and kisspeptin as opposing forces in regulating pubertal timing. LD-induced melatonin suppression allows the kisspeptin symphony to flourish, triggering GnRH release and, ultimately, gonadal maturation. 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Decoding the effect of photoperiodic cues in transducing kisspeptin-melatonin circuit during the pubertal onset in common carp
This study unravels the intricate interplay between photoperiod, melatonin, and kisspeptin to orchestrate the pubertal onset of Common carp. Female fingerlings exposed to long days (LD) exhibited a hormonal crescendo, with upregulated hypothalamic-pituitary-ovarian (HPO) axis genes (kiss1, kiss1r, kiss2, gnrh2, gnrh3) and their downstream targets (lhr, fshr, ar1, esr1). However, the expression of the melatonin receptor (mtnr1a) diminished in LD, suggesting a potential inhibitory role. This hormonal symphony was further amplified by increased activity of key transcriptional regulators (gata1, gata2, cdx1, sp1, n-myc, hoxc8, plc, tac3, tacr3) and decreased expression of delayed puberty genes (mkrn1, dlk1). In contrast, short days (SD) muted this hormonal chorus, with decreased gnrh gene and regulator expression, elevated mtnr1a, and suppressed gonadal development. In in-vitro, estradiol mimicked the LD effect, boosting gnrh and regulator genes while dampening mtnr1a and melatonin-responsive genes. Conversely, melatonin acted as a conductor, downregulating gnrh and regulator genes and amplifying mtnr1a. Our findings illuminate the crucial roles of melatonin and kisspeptin as opposing forces in regulating pubertal timing. LD-induced melatonin suppression allows the kisspeptin symphony to flourish, triggering GnRH release and, ultimately, gonadal maturation. This delicate dance between photoperiod, melatonin, and kisspeptin orchestrates common carp's transition from juvenile to reproductive life.
期刊介绍:
Molecular Reproduction and Development takes an integrated, systems-biology approach to understand the dynamic continuum of cellular, reproductive, and developmental processes. This journal fosters dialogue among diverse disciplines through primary research communications and educational forums, with the philosophy that fundamental findings within the life sciences result from a convergence of disciplines.
Increasingly, readers of the Journal need to be informed of diverse, yet integrated, topics impinging on their areas of interest. This requires an expansion in thinking towards non-traditional, interdisciplinary experimental design and data analysis.