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杂交组织化学:使用重组DNA作为“归巢探针”对特定mRNA群体进行组织定位。

Hybridization histochemistry: use of recombinant DNA as a "homing probe" for tissue localization of specific mRNA populations.

作者信息

Hudson P, Penschow J, Shine J, Ryan G, Niall H, Coghlan J

出版信息

Endocrinology. 1981 Jan;108(1):353-6. doi: 10.1210/endo-108-1-353.

Abstract

A procedure, termed hybridization histochemistry, has been developed to locate in specially prepared whole sections of tissue those areas which contain specific mRNA populations. Three 32P-labelled recombinant DNA probes were used; one complementary to endorphin mRNA, one complementary to growth hormone mRNA and one a fragment of bacterial DNA. The specific cell populations or tissue regions binding the probe were identified by autoradiography. Hybridization histochemistry is thus similar in principle to immunohistochemical procedures. The endorphin probe consistently labelled the rat pituitary pars intermedia which is known to be particularly rich in the corresponding mRNA. Likewise the growth hormone probe specifically labelled the anterior pituitary. Control tissues were not labelled by either probe, nor did the bacterial DNA probe significantly label any tissue, providing further evidence of the specificity of the procedure. These results, which are highly reproducible, indicate that the mRNA species for endorphin and growth hormone are present in whole sections of pituitary in a physical state which leaves them accessible to cDNA probes. This initial success provides encouragement that hybridization histochemistry, with further refinement, should have wide applicability in the localization and semi-quantitative analysis of intracellular mRNA in whole frozen sections of tissue.

摘要

一种称为杂交组织化学的方法已被开发出来,用于在经过特殊制备的组织全切片中定位那些含有特定mRNA群体的区域。使用了三种32P标记的重组DNA探针;一种与内啡肽mRNA互补,一种与生长激素mRNA互补,还有一种是细菌DNA片段。通过放射自显影鉴定与探针结合的特定细胞群体或组织区域。因此,杂交组织化学在原理上与免疫组织化学方法相似。内啡肽探针始终标记大鼠垂体中间部,已知该部位富含相应的mRNA。同样,生长激素探针特异性地标记垂体前叶。对照组织均未被任何一种探针标记,细菌DNA探针也未显著标记任何组织,这进一步证明了该方法的特异性。这些结果具有高度的可重复性,表明内啡肽和生长激素的mRNA种类以一种能被cDNA探针识别的物理状态存在于垂体全切片中。这一初步成功令人鼓舞,表明经过进一步改进,杂交组织化学在组织全冷冻切片中细胞内mRNA的定位和半定量分析方面应具有广泛的适用性。

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