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新的小鼠连接蛋白39基因在发育中的横纹肌纤维中表达。

The novel mouse connexin39 gene is expressed in developing striated muscle fibers.

作者信息

von Maltzahn Julia, Euwens Carsten, Willecke Klaus, Söhl Goran

机构信息

Institut für Genetik, Abteilung Molekulargenetik, Universität Bonn, Römerstr. 164, 53117 Bonn, Germany.

出版信息

J Cell Sci. 2004 Oct 15;117(Pt 22):5381-92. doi: 10.1242/jcs.01413. Epub 2004 Oct 5.

DOI:10.1242/jcs.01413
PMID:15466892
Abstract

The recently identified mouse connexin39 (mCx39) gene encodes a peptide of 364 amino acids that shows only 61% sequence similarity to its putative human orthologue connexin40.1 (hCx40.1). The coding regions of mCx39 and hCx40.1 are located on two different exons as described for murine and human connexin36. Northern blot and RT-PCR analyses revealed that mCx39 is expressed after embryonic day (ED) 13.5 up to birth and is absent from the adult stage. Polyclonal antibodies raised to a peptide corresponding to the 16 C-terminal amino acid residues detected a protein band of about 40 kDa apparent molecular mass in lysates of several embryonic tissues. In sections of ED14.5, ED16.5 and neonatal (P0) tissues, immunofluorescent signals were prominent between myotubes in the developing diaphragm, within the intercostal muscle, in the region around the occipital bone, as well as in muscles of the limb, tongue and connective tissue around the eye. These antibodies yielded punctate signals on apposed plasma membranes of HeLa cells transfected with Cx39 cDNA but did not react with wild-type cells. Furthermore, no intercellular permeation of microinjected neurobiotin and other tracers could be detected in Cx39 transfected HeLa cells. However, after microinjection of Alexa488 into myotubes of dissected neonatal diaphragm, we found spreading of this dye into neighbouring cells. As expression of no other known connexin could be verified in these cells, intercellular dye transfer might result from functional expression of Cx39 in developing striated muscle fibers.

摘要

最近鉴定出的小鼠连接蛋白39(mCx39)基因编码一种由364个氨基酸组成的肽,该肽与推测的人类同源物连接蛋白40.1(hCx40.1)仅具有61%的序列相似性。如对小鼠和人类连接蛋白36的描述,mCx39和hCx40.1的编码区位于两个不同的外显子上。Northern印迹和RT-PCR分析表明,mCx39在胚胎期第13.5天(ED 13.5)后至出生时表达,成年期不存在。针对对应于16个C末端氨基酸残基的肽产生的多克隆抗体在几种胚胎组织的裂解物中检测到一条表观分子量约为40 kDa的蛋白条带。在ED14.5、ED16.5和新生(P0)组织切片中,免疫荧光信号在发育中的膈肌肌管之间、肋间肌内、枕骨周围区域以及肢体、舌头和眼周围结缔组织的肌肉中很明显。这些抗体在用Cx39 cDNA转染的HeLa细胞的相对质膜上产生点状信号,但不与野生型细胞反应。此外,在转染Cx39的HeLa细胞中未检测到微注射的神经生物素和其他示踪剂的细胞间渗透。然而,在将Alexa488微注射到解剖的新生膈肌的肌管中后,我们发现这种染料扩散到了相邻细胞中。由于在这些细胞中未证实其他已知连接蛋白的表达,细胞间染料转移可能是由于Cx39在发育中的横纹肌纤维中的功能性表达所致。

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