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存在一种可能控制小鼠肠道蔗糖酶表达的调控基因(Suc-1)的证据。

Evidence for a possible regulatory gene (Suc-1) controlling sucrase expression in mouse intestine.

作者信息

James P S, Smith M W, Butcher G W, Brown D, Lund E K

出版信息

Biochem Genet. 1986 Apr;24(3-4):169-81. doi: 10.1007/BF00502786.

DOI:10.1007/BF00502786
PMID:3729924
Abstract

Assays for sucrase carried out on intestinal sonicates prepared from 18 different strains of mice revealed a threefold variation in specific activity, the values for CBA/Ca mice being significantly less than for any other strain. Further comparison of the CBA/Ca versus the C57BL/6J mouse showed this deficiency, which became established 2-4 weeks after birth, to apply to isomaltase as well as sucrase but not to maltase or trehalase. Backcross experiments indicated that this deficiency in sucrase activity was inherited as a single codominantly expressed genetic factor. The ability of the CBA/Ca mouse to regulate sucrase activity in response to changes in diet was also reduced compared to that of the C57BL/6J mouse. No difference could be detected in the affinity of sucrase for its substrate or in the ability of heat to denature sucrase prepared from CBA/Ca and C57BL/6J mice. It is suggested that part of the regulatory region of the gene coding for sucrase-isomaltase is modified in the CBA/Ca mouse and that this locus should be given the notation Suc-1 for future reference.

摘要

对从18种不同品系小鼠制备的肠超声匀浆进行的蔗糖酶测定显示,比活性有三倍的差异,CBA/Ca小鼠的值显著低于任何其他品系。对CBA/Ca小鼠与C57BL/6J小鼠的进一步比较表明,这种在出生后2至4周确立的缺陷适用于异麦芽糖酶和蔗糖酶,但不适用于麦芽糖酶或海藻糖酶。回交实验表明,蔗糖酶活性的这种缺陷作为一个单一的共显性表达遗传因子遗传。与C57BL/6J小鼠相比,CBA/Ca小鼠响应饮食变化调节蔗糖酶活性的能力也降低。在蔗糖酶对其底物的亲和力或热变性CBA/Ca和C57BL/6J小鼠制备的蔗糖酶的能力方面未检测到差异。有人提出,编码蔗糖酶-异麦芽糖酶的基因的部分调控区域在CBA/Ca小鼠中发生了改变,并且该基因座应标记为Suc-1以供将来参考。

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Evidence for a possible regulatory gene (Suc-1) controlling sucrase expression in mouse intestine.存在一种可能控制小鼠肠道蔗糖酶表达的调控基因(Suc-1)的证据。
Biochem Genet. 1986 Apr;24(3-4):169-81. doi: 10.1007/BF00502786.
2
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引用本文的文献

1
The sucrase-isomaltase structural gene (Si-s) and a regulatory gene (Si-r) are closely linked to esterase-26 (Es-26) on mouse chromosome 3.蔗糖酶-异麦芽糖酶结构基因(Si-s)和一个调控基因(Si-r)与小鼠3号染色体上的酯酶-26(Es-26)紧密连锁。
Mamm Genome. 1993 Sep;4(9):531-6. doi: 10.1007/BF00364789.
2
Regulatory and structural genes for lysozymes of mice.小鼠溶菌酶的调控基因和结构基因。
Genetics. 1987 Mar;115(3):521-33. doi: 10.1093/genetics/115.3.521.

本文引用的文献

1
INTESTINAL INVERTASE: PRECOCIOUS DEVELOPMENT OF ACTIVITY AFTER INJECTION OF HYDROCORTISONE.肠蔗糖酶:注射氢化可的松后活性的早熟发育。
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Specificity of the human intestinal disaccharidases and implications for hereditary disaccharide intolerance.人类肠道双糖酶的特异性及其对遗传性双糖不耐受的影响。
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Comparative in vivo and in vitro effect of mono- and disaccharides on intestinal brush border enzyme activities in suckling rats.
单糖和双糖对乳鼠肠道刷状缘酶活性的体内和体外比较效应
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4
Monoclonal antibodies to mouse MHC antigens. III. Hybridoma antibodies reacting to antigens of the H-2b haplotype reveal genetic control of isotype expression.抗小鼠主要组织相容性复合体(MHC)抗原的单克隆抗体。III. 与H-2b单倍型抗原发生反应的杂交瘤抗体揭示了同种型表达的遗传控制。
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Lactase polymorphism in adult British natives: estimating allele frequencies by enzyme assays in autopsy samples.英国成年本土居民的乳糖酶多态性:通过尸检样本中的酶测定估算等位基因频率。
Am J Hum Genet. 1982 Jul;34(4):650-7.
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Increased activity of rat intestinal lactase due to increased intake of alpha-saccharides (starch, sucrose) in isocaloric diets.在等热量饮食中,由于α-糖类(淀粉、蔗糖)摄入量增加,大鼠肠道乳糖酶活性增强。
J Nutr. 1981 Jun;111(6):943-53. doi: 10.1093/jn/111.6.943.
7
Biosynthesis of intestinal microvillar proteins. Intracellular processing of lactase-phlorizin hydrolase.肠道微绒毛蛋白的生物合成。乳糖酶-根皮苷水解酶的细胞内加工过程。
Biochem Biophys Res Commun. 1984 Jul 18;122(1):82-90. doi: 10.1016/0006-291x(84)90442-x.
8
Gene-dosage effect on intestinal lactase activity demonstrated in vivo.体内证实的基因剂量对肠道乳糖酶活性的影响。
Am J Hum Genet. 1984 Mar;36(2):306-10.
9
Biosynthesis of intestinal microvillar proteins. Pulse-chase labelling studies on maltase-glucoamylase, aminopeptidase A and dipeptidyl peptidase IV.肠道微绒毛蛋白的生物合成。对麦芽糖酶-葡糖淀粉酶、氨肽酶A和二肽基肽酶IV的脉冲追踪标记研究。
Biochem J. 1983 Feb 15;210(2):389-93. doi: 10.1042/bj2100389.
10
Mep-1 gene controlling a kidney metalloendopeptidase is linked to the major histocompatibility complex in mice.控制肾脏金属内肽酶的Mep-1基因与小鼠的主要组织相容性复合体相关联。
Proc Natl Acad Sci U S A. 1984 Sep;81(17):5542-5. doi: 10.1073/pnas.81.17.5542.