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利用重酶解肌球蛋白结合和十二烷基硫酸钠聚丙烯酰胺凝胶电泳对心脏致死突变型墨西哥钝口螈(美西螈)胚胎心肌细胞中的肌肉蛋白进行研究。

Studies of muscle proteins in embryonic myocardial cells of cardiac lethal mutant mexican axolotls (Ambystoma mexicanum) by use of heavy meromyosin binding and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

作者信息

Lemanski L F, Mooseker M S, Peachey L D, Iyengar M R

出版信息

J Cell Biol. 1976 Feb;68(2):375-88. doi: 10.1083/jcb.68.2.375.

Abstract

In the Mexican axolotl Ambystoma mexicanum recessive mutant gene c, by way of abnormal inductive processes from surrounding tissues, results in an absence of embryonic heart function. The lack of contractions in mutant heart cells apparently results from their inability to form normally organized myofibrils, even though a few actin-like (60-A) and myosin-like (150-A) filaments are present. Amorphous "proteinaceous" collections are often visible. In the present study, heavy meromyosin (HMM) treatment of mutant heart tissue greatly increases the number of thin filaments and decorates them in the usual fashion, confirming that they are actin. The amorphous collections disappear with the addition of HMM. In addition, an analysis of the constituent proteins of normal and mutant embryonic hearts and other tissues is made by sodium dodecyl sulfate (SDS) gel electrophoresis. These experiments are in full agreement with the morphological and HMM binding studies. The gels show distinct 42,000-dalton bands for both normal and mutant hearts, supporting the presence of normal actin. During early developmental stages (Harrison's stage 34) the cardiac tissues in normal and mutant siblings have indistinguishable banding patterns, but with increasing development several differences appear. Myosin heavy chain (200,000 daltons) increases substantially in normal hearts during development but very little in mutants. Even so the quantity of 200,000-dalton protein in mutant hearts is significantly more than in any of the nonmuscle tissues studied (i.e. gut, liver, brain). Unlike normal hearts, the mutant hearts lack a prominent 34,000-dalton band, indicating that if mutants contain muscle tropomyosin at all, it is present in drastically reduced amounts. Also, mutant hearts retain large amounts of yolk proteins at stages when the platelets have virtually disappeared from normal hearts. The morphologies and electrophoresis patterns of skeletal muscle from normal and mutant siblings are identical, confirming that gene c affects only heart muscle differentiation and not skeletal muscle. The results of the study suggest that the precardiac mesoderm in cardiac lethal mutant axolotl embryos initiates but then fails to complete its differentiation into functional muscle tissue. It appears that this single gene mutation, by way of abnormal inductive processes, affects the accumulation and organization of several different muscle proteins, including actin, myosin, and tropomyosin.

摘要

在墨西哥钝口螈(美西螈)中,隐性突变基因c通过周围组织异常的诱导过程,导致胚胎心脏功能缺失。突变心脏细胞缺乏收缩能力显然是由于它们无法形成正常排列的肌原纤维,尽管存在一些肌动蛋白样(60埃)和肌球蛋白样(150埃)细丝。无定形的“蛋白质样”聚集体常常可见。在本研究中,用重酶解肌球蛋白(HMM)处理突变心脏组织可显著增加细肌丝的数量,并以常规方式使其显影,证实它们是肌动蛋白。添加HMM后,无定形聚集体消失。此外,通过十二烷基硫酸钠(SDS)凝胶电泳对正常和突变胚胎心脏及其他组织的组成蛋白进行了分析。这些实验与形态学和HMM结合研究完全一致。凝胶显示正常和突变心脏都有明显的42,000道尔顿条带,支持正常肌动蛋白的存在。在发育早期阶段(哈里森第34期),正常和突变同胞的心脏组织具有难以区分的条带模式,但随着发育的进行出现了一些差异。正常心脏在发育过程中肌球蛋白重链(200,000道尔顿)显著增加,而突变体中增加很少。即便如此,突变心脏中200,000道尔顿蛋白质的量仍明显多于所研究的任何非肌肉组织(即肠道、肝脏、大脑)。与正常心脏不同,突变心脏缺乏一条突出的34,000道尔顿条带,这表明如果突变体含有肌肉原肌球蛋白的话,其含量也大幅减少。此外,在正常心脏中血小板几乎消失的阶段,突变心脏仍保留大量卵黄蛋白。正常和突变同胞的骨骼肌形态和电泳图谱相同,证实基因c仅影响心肌分化,而不影响骨骼肌。研究结果表明,心脏致死突变钝口螈胚胎中的心脏前中胚层启动了分化,但随后未能完成向功能性肌肉组织的分化。看来这个单一基因突变通过异常的诱导过程,影响了几种不同肌肉蛋白的积累和组织,包括肌动蛋白、肌球蛋白和原肌球蛋白。

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