Molecular characterization of an additional shrimp hyperglycemic hormone: cDNA cloning, gene organization, expression and biological assay of recombinant proteins 1

• Published in: FEBS letters Vol. 472; no. 1; pp. 122 - 128
• Main Authors: Gu, Pei-Li, Yu, Kei Li, Chan, Siu-Ming
• Format: Journal Article
• Language: English
• Published: 21.04.2000
• Subjects: CHH, crustacean hyperglycemic hormone; Crustacean hyperglycemic hormone; Gene organization; GIH, gonad inhibiting hormone; MIH, molt inhibiting hormone; RT-PCR, reverse transcription polymerase chain reaction; Shrimp
• ISSN: 0014-5793; 1873-3468
• DOI: 10.1016/S0014-5793(00)01420-4

The crustacean eyestalk CHH/MIH/GIH neurohormone gene family represents a unique group of neuropeptides identified mainly in crustaceans. In this study, we report the cloning and characterization of the cDNA and the gene encoding the hyperglycemic hormone (MeCHH‐B) of the shrimp Metapenaeus ensis. The amino acid sequence of MeCHH‐B shows 85% identity to that of MeCHH‐A (formerly MeCHH‐like neuropeptide). Two separate but identical MeCHH‐B genes were identified in the genome of shrimp by library screening and they are located on different CHH gene clusters. The organization of the MeCHH‐B gene is identical to other members of the CHH/MIH/GIH neurohormone family. MeCHH‐B is expressed at a constant level in the eyestalks of juveniles and mature females. Unlike the MeCHH‐A gene, a low level of MeCHH‐B transcripts can also be detected in the central nervous system. Interestingly, the expression pattern of MeCHH‐B in the eyestalk of vitellogenic females is reversed to that of the MeCHH‐A gene. At the middle stage of gonad maturation, a minimum level of MeCHH‐B transcript was recorded and a maximum level of MeCHH‐A transcript was detected. Recombinant proteins for MeCHH‐A and MeCHH‐B were produced by a bacterial expression system. The hemolymph glucose level of bilaterally eyestalk‐ablated shrimp increased two‐fold 1 h after the rCHH injection and then returned to normal after 2 h. The hyperglycemic effect of these fusion proteins is comparable to that of de‐stalked shrimp injected with crude extract from a single sinus gland.