ZFIN ID: ZDB-PUB-200530-14
Ectopic over expression of kiss1 may compensate for the loss of kiss2
Talya, E., Nilli, Z., Yonatan, Z., Berta, L.S., Matan, G., Yoav, G.
Date: 2020
Source: General and comparative endocrinology   295: 113523 (Journal)
Registered Authors: Gothilf, Yoav
Keywords: Compensatory mechanism, Kisspeptin, Knockout, Reproduction, Tachykinin, Zebrafish
MeSH Terms:
  • Animals
  • Base Sequence
  • Brain/metabolism
  • Female
  • Gene Expression Regulation
  • Gene Knockout Techniques
  • Gonadotropins/genetics
  • Gonadotropins/metabolism
  • Kisspeptins/metabolism*
  • Male
  • Mutation/genetics
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Reproduction/genetics
  • Zebrafish/metabolism*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed: 32470472 Full text @ Gen. Comp. Endocrinol.
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ABSTRACT
Kisspeptin (KISS) is a neuropeptide which plays a central role in the regulation of the hypothalamic-pituitary-gonadal axis, and is essential for sexual maturation and fertility in mammals. Unlike mammals, which possess only one KISS gene, two paralogous genes, kiss1 and kiss2, have been identified in zebrafish and other non-mammalian vertebrates. Previous studies suggest that Kiss2, but not Kiss1, is the reproduction relevant form amongst the two. To better understand the role of each of these isoforms in reproduction, a loss of function approach was applied. Two genetic manipulation techniques-clustered regularly interspaced short palindromic repeats (CRISPR) and transcription activator-like effector nucleases (TALEN)-were used to generate kiss1 and kiss2 knockout (KO) zebrafish lines, respectively. Examination of these KO lines showed that reproductive capability was not impaired, confirming earlier observations. Further analysis revealed that KO of kiss2 caused a significant increase in expression levels of kiss1, kiss2r and tac3a, while KO of kiss1 had no effect on the expression of any of the examined genes. In situ hybridization analysis revealed that kiss1 mRNA is expressed only in the habenula in wild type brains, while in kiss2 KO fish, kiss1 mRNA-expressing cells were identified also in the ventral telencephalon, the ventral part of the entopeduncular nucleus, and the dorsal and ventral hypothalamus. Interestingly, these regions are known to express kiss2r, and the ventral hypothalamus normally expresses kiss2. These results suggest that a compensatory mechanism, involving ectopic kiss1 expression, takes place in the kiss2 KO fish, which may substitute for Kiss2 activity.
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