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在大脑发育过程中鉴定和描述 PLEKHA5(Plekha5)的剪接变体。

Identification and characterization of splicing variants of PLEKHA5 (Plekha5) during brain development.

机构信息

Department of Genetics, Institute for Developmental Research, Aichi Human Service Center, Aichi, Japan.

出版信息

Gene. 2012 Jan 15;492(1):270-5. doi: 10.1016/j.gene.2011.10.018. Epub 2011 Oct 20.

Abstract

PLEKHA5 (pleckstrin homology domain-containing protein family A, member 5) belongs to the PLEKHA family (PLEKHA1-6); however, the properties of this protein remain poorly characterized. We have identified and characterized two forms of PLEKHA5 mRNA. The long form of PLEKHA5 (L-PLEKHA5) contains 32 exons, encodes 1282 amino acids, and is specifically expressed in the brain; the short form of PLEKHA5 (S-PLEKHA5) is generated by alternative splicing of L-PLEKHA5, contains 26 exons, encodes 1116 amino acids, and is ubiquitously expressed. Both forms of the protein contain putative Trp-Trp (WW) and pleckstrin homology (PH) domains and are located mainly in the cytosol. Developmental and age-dependent expression studies in the mouse brain have shown that Plekha5 is the most abundantly expressed protein at E13.5 with S-Plekha5 dominancy. L-Plekha5 levels increased gradually with the decrease in total Plekha5 levels; moreover, L-Plekha5 became the dominant protein at E17.5, maintaining its dominance throughout adulthood. Protein-lipid overlay assays have indicated that the PH domain of PLEKHA5 specifically interacts with PI3P, PI4P, PI5P, and PI(3,5)P2. These results suggest that the S- to L-conversion of PLEKHA5 (Plekha5) may play an important role in brain development through association with specific phosphoinositides.

摘要

PLEKHA5(pleckstrin homology 结构域家族 A,成员 5)属于 PLEKHA 家族(PLEKHA1-6);然而,这种蛋白质的特性仍未得到很好的描述。我们已经鉴定和表征了两种 PLEKHA5 mRNA 形式。长形式的 PLEKHA5(L-PLEKHA5)包含 32 个外显子,编码 1282 个氨基酸,特异性表达于脑内;短形式的 PLEKHA5(S-PLEKHA5)是通过 L-PLEKHA5 的选择性剪接产生的,包含 26 个外显子,编码 1116 个氨基酸,广泛表达。这两种形式的蛋白质都含有潜在的色氨酸-色氨酸(WW)和 pleckstrin homology(PH)结构域,主要位于细胞质中。在小鼠脑中进行的发育和年龄依赖性表达研究表明,Plekha5 在 E13.5 时表达最为丰富,以 S-Plekha5 为主导。L-Plekha5 水平随着总 Plekha5 水平的降低而逐渐增加;此外,L-Plekha5 在 E17.5 时成为优势蛋白,并在整个成年期保持其主导地位。蛋白-脂质覆盖实验表明,PLEKHA5 的 PH 结构域特异性地与 PI3P、PI4P、PI5P 和 PI(3,5)P2 相互作用。这些结果表明,PLEKHA5(Plekha5)的 S 到 L 的转换可能通过与特定的磷酸肌醇结合在大脑发育中发挥重要作用。

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