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分子遗传学——血液学的新视野。

Molecular genetics--new horizons in haematology.

作者信息

Hollán S

机构信息

National Institute of Haematology and Blood Transfusion, Budapest, Hungary.

出版信息

Haematologia (Budap). 1991;24(3):167-88.

PMID:1726792
Abstract

The unprecedentedly swift developments in molecular genetics has opened up a new era in biology and medicine. The powerful methods of recombinant DNA (rDNA) technology are fast moving into the fields of diagnostics and therapy since the newly found ability to define physiological and pathological cell functions at a molecular level. The centerpiece of molecular genetics is the possibility to map and determine the fine structure of human genes and to define in molecular terms how each gene controls all the enzymes of energy metabolism, structural proteins of cells, the membrane proteins, including transport proteins and receptors, the plasma proteins and those proteins which participate in the synthesis of complex lipids, carbohydrates, lipoproteins and glycoproteins. The fundamental change of emphasis in cellular and clinical research in medicine started in haematology. No wonder, since the circulating blood cells, the bone marrow, and lymphoid tissue cells are easily available for investigation and most of the haematological diseases are well defined entities. This review will try to present the increasing depth and broadening spectrum of molecular haematology by arbitrary chosen examples: 1) Molecular regulation of cell specific gene expression and of age specific switch of the globin genes, 2) Revisiting the haemolysis of paroxysmal nocturnal haemoglobinuria (PNH) cells--the phosphatidylinositol-glycan (PIG) anchored membrane proteins, 3) Molecular genetics of the ABO and Rh blood group specificity, 4) The regulation of stem cells and the multistep process of their malignant transformation. 5) The impact of gene technology on diagnostics, prevention and therapy in haematology, 6) The present state of art and future possibilities of the treatment of genetic diseases.

摘要

分子遗传学前所未有的迅猛发展开启了生物学和医学的新纪元。重组DNA(rDNA)技术的强大方法正迅速进入诊断和治疗领域,因为人们新发现了在分子水平定义生理和病理细胞功能的能力。分子遗传学的核心在于能够绘制并确定人类基因的精细结构,并从分子角度定义每个基因如何控制能量代谢的所有酶、细胞的结构蛋白、膜蛋白(包括转运蛋白和受体)、血浆蛋白以及参与复合脂质、碳水化合物、脂蛋白和糖蛋白合成的那些蛋白。医学中细胞和临床研究重点的根本转变始于血液学领域。这并不奇怪,因为循环血细胞、骨髓和淋巴组织细胞易于获取用于研究,而且大多数血液学疾病都是明确的实体。本综述将通过任意选取的例子来呈现分子血液学不断加深的深度和不断拓宽的范围:1)细胞特异性基因表达和珠蛋白基因年龄特异性转换的分子调控;2)重新审视阵发性夜间血红蛋白尿(PNH)细胞的溶血——磷脂酰肌醇聚糖(PIG)锚定膜蛋白;3)ABO和Rh血型特异性的分子遗传学;4)干细胞的调控及其恶性转化的多步骤过程;5)基因技术对血液学诊断、预防和治疗的影响;6)遗传疾病治疗的现状和未来可能性。

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