The transcriptional regulatory strategy of the rat tissue kallikrein gene family

Evert Kroon, Raymond MacDonald, Robert Hammer
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引用次数: 9

Abstract

We have analysed the transcriptional regulatory strategy of the rat tissue kallikrein gene family, a strategy that provides universal submandibular gland expression of all family members coupled with otherwise disparate expression of individual members in a wide variety of organs. To test whether a locus control region (LCR) or individual gene enhancers control the family, the expression patterns of rat kallikrein genes were examined in transgenic mice bearing a series of rat genomic fragments spanning the kallikrein locus. Each fragment, present in recombinant P1 phage clones, contained two or three linked members of the rat family. Rat (r) genes KLK1, KLK2, KLK3, KLK7, KLK8, KLK9 and KLK10 on four different P1 clones were all correctly expressed at high levels in the submandibular glands of transgenic mice and in general showed the correct extra-salivary patterns characteristic of each family member. Moreover, when the neighbouring family members rKLK1 and rKLK3 were separated on non-overlapping fragments and tested in mice, each transgene was expressed correctly in the submandibular gland and in other organs characteristic of that gene. Thus the family locus is not controlled by an LCR; rather each gene appears to have an associated transcriptional enhancer that specifies high submandibular expression and contributes to the additional organ specificity of the family member.

大鼠组织激肽激酶基因家族的转录调控策略
我们分析了大鼠组织激肽激酶基因家族的转录调控策略,该策略提供了所有家族成员的普遍下颌腺表达,以及各种器官中个体成员的不同表达。为了测试是基因座控制区(LCR)还是单个基因增强子控制了这个家族,我们在携带一系列跨越基因座的大鼠基因组片段的转基因小鼠中检测了大鼠激肽激酶基因的表达模式。每个片段,存在于重组P1噬菌体克隆中,包含两个或三个大鼠家族的连锁成员。4个不同P1克隆的大鼠(r)基因KLK1、KLK2、KLK3、KLK7、KLK8、KLK9和KLK10在转基因小鼠的下颌下腺中均正确高水平表达,总体上显示出每个家族成员所特有的正确的唾液外模式。此外,当邻近的家族成员rKLK1和rKLK3在不重叠的片段上分离并在小鼠中进行测试时,每个转基因在颌下腺和该基因特征的其他器官中都正确表达。因此,家族位点不受LCR控制;相反,每个基因似乎都有一个相关的转录增强子,该转录增强子指定下颌下高表达,并有助于家庭成员的额外器官特异性。
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