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c-akt的类SH2的Akt同源(AH)结构域在脊椎动物和无脊椎动物真核生物的基因组中以多个拷贝存在。果蝇c-akt同源物Dakt1的克隆与鉴定。

The SH2-like Akt homology (AH) domain of c-akt is present in multiple copies in the genome of vertebrate and invertebrate eucaryotes. Cloning and characterization of the Drosophila melanogaster c-akt homolog Dakt1.

作者信息

Franke T F, Tartof K D, Tsichlis P N

机构信息

Fox Chase Cancer Center, Philadelphia, PA 19111.

出版信息

Oncogene. 1994 Jan;9(1):141-8.

PMID:8302573
Abstract

The Akt proto-oncogene encodes a serine-threonine protein kinase whose carboxyterminal catalytic domain is closely related to the catalytic domains of all the known members of the protein kinase C (PKC) family. Akt, however, differs from PKC in its N-terminal region which contains a domain related distantly to the SH2 domain of cytoplasmic tyrosine kinases and other signalling proteins, which we have named Akt homology (AH) domain. Low stringency hybridization of a c-akt AH probe to a panel of genomic DNAs from vertebrate and invertebrate eucaryotes detected multiple DNA bands (perhaps multiple genes) in all tested species. Drosophila DNA contains at least three hybridizing DNA bands. One of them was cloned, and found by sequence analysis, to define an Akt related gene (Dakt1). Comparison between the coding regions of c-akt and Dakt1 revealed 64.6% identity at the nucleotide level and 76.5% similarity at the amino acid level. The highest degree of homology was detected in the AH domain (68.3% similarity at the amino acid level) and the catalytic domain (83.3% similarity). Additional sequence comparisons revealed that the amino acid similarity between the catalytic domains of Dkt1 and the three known members of the Drosophila protein kinase C (PKC) family, Dpkc1, Dpkc2 and Dpkc3, is 68%, 63.6% and 67.1%, respectively. Dakt1 was mapped to Drosophila chromosome 3R 89BC. Its expression is subject to developmental regulation with the highest levels detected within the fourth hour of embryonic development. These results confirm that the AH domain of Akt defines new protein families in both vertebrate and invertebrate eucaryotes. The high degree of homology between the catalytic domains of Dkt1 and the three known members of the Drosophila PKC family suggests an evolutionarily conserved functional relationship between the members of the two families.

摘要

Akt原癌基因编码一种丝氨酸 - 苏氨酸蛋白激酶,其羧基末端催化结构域与蛋白激酶C(PKC)家族所有已知成员的催化结构域密切相关。然而,Akt在其N末端区域与PKC不同,该区域包含一个与细胞质酪氨酸激酶和其他信号蛋白的SH2结构域有远缘关系的结构域,我们将其命名为Akt同源(AH)结构域。用c-akt AH探针与一组来自脊椎动物和无脊椎动物真核生物的基因组DNA进行低严谨度杂交,在所有测试物种中检测到多个DNA条带(可能是多个基因)。果蝇DNA至少包含三个杂交DNA条带。其中一个被克隆,并通过序列分析发现它定义了一个与Akt相关的基因(Dakt1)。c-akt和Dakt1编码区之间的比较显示,核苷酸水平上的同一性为64.6%,氨基酸水平上的相似性为76.5%。在AH结构域(氨基酸水平上相似性为68.3%)和催化结构域(相似性为83.3%)中检测到最高程度的同源性。进一步的序列比较表明,Dkt1催化结构域与果蝇蛋白激酶C(PKC)家族的三个已知成员Dpkc1、Dpkc2和Dpkc3之间的氨基酸相似性分别为68%、63.6%和67.1%。Dakt1被定位到果蝇3R 89BC染色体上。其表达受发育调控,在胚胎发育的第四小时检测到最高水平。这些结果证实,Akt的AH结构域在脊椎动物和无脊椎动物真核生物中都定义了新的蛋白家族。Dkt1催化结构域与果蝇PKC家族的三个已知成员之间的高度同源性表明这两个家族成员之间存在进化上保守的功能关系。

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