characterization and expression of glutamate dehydrogenase in response to acute salinity stress in the chinese mitten crab, eriocheir sinensis表征和谷氨酸脱氢酶的表达,以应对急性盐度压力在中华绒螯蟹,中华绒螯蟹.pdfVIP
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characterization and expression of glutamate dehydrogenase in response to acute salinity stress in the chinese mitten crab, eriocheir sinensis表征和谷氨酸脱氢酶的表达,以应对急性盐度压力在中华绒螯蟹,中华绒螯蟹
Characterization and Expression of Glutamate
Dehydrogenase in Response to Acute Salinity Stress in
the Chinese Mitten Crab, Eriocheir sinensis
1 1 1 1 2 3 1
Yueru Wang , Erchao Li *, Na Yu , Xiaodan Wang , Chunfang Cai , Boping Tang , Liqiao Chen *,
Alain Van Wormhoudt4
1 School of Life Science, East China Normal University, Shanghai, China, 2 School of Basic Medicine and Biological Science, Soochow University, Suzhou, China, 3 Jiangsu
Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection, School of Basic Medicine and Biological Science, Yancheng Teachers University,
´
Yancheng, China, 4 UMR5178, Station de Biologie Marine du Museum National d’Histoire Naturelle, BP225, Concarneau, France
Abstract
Background: Glutamate dehydrogenase (GDH) is a key enzyme for the synthesis and catabolism of glutamic acid, proline
and alanine, which are important osmolytes in aquatic animals. However, the response of GDH gene expression to salinity
alterations has not yet been determined in macro-crustacean species.
Methodology/Principal Findings: GDH cDNA was isolated from Eriocheir sinensis. Then, GDH gene expression was analyzed
in different tissues from normal crabs and the muscle of crabs following transfer from freshwater (control) directly to water
with salinities of 16% and 30%, respectively. Full-length GDH cDNA is 2,349 bp, consisting of a 76 bp 5 9- untranslated
region, a 1,695 bp open reading frame encoding 564 amino acids and a 578 bp 39- untranslated region. E. sinensis GDH
showed 64–90% identity with protein sequences of mammalian and crustacean species. Muscle was the dominant
expression source among
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