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下丘脑性尿崩症大鼠 Walker 256 癌肉瘤退行模式的遗传决定。

Genetic Determination of Regressive Pattern of Walker 256 Carcinosarcoma in Rats with Hypothalamic Diabetes Insipidus.

机构信息

Federal Research Center Institute of Cytology and Genetics, Siberian Division of the Russian Academy of Sciences, Novosibirsk, Russia.

出版信息

Bull Exp Biol Med. 2022 Aug;173(4):441-443. doi: 10.1007/s10517-022-05583-3. Epub 2022 Sep 5.

Abstract

We studied the growth dynamics of Walker 256 carcinosarcoma in recombinant progeny of dihybrid crosses of Brattleboro and WAG rats. A mutation in the vasopressin gene determining hypothalamic diabetes insipidus was detected in Brattleboro rats. WAG rats are carriers of normal vasopressin gene. Another interlinear difference was linked to tyrosinase gene controlling melanin synthesis. WAG rats express mutant allele determining albino phenotype. Brattleboro rats had normal working tyrosinase gene. F2 segregation yielded phenotypic classes with two patterns of tumor growth: linear growth or regression. Tumors regression was not linked to tyrosinase activity and was observed only in rats with diabetes insipidus. Analysis of mutants in next generations F3 and F4 confirmed this regularity in the Walker 256 carcinosarcoma growth pattern.

摘要

我们研究了 Brattleboro 和 WAG 大鼠杂交后代重组种系中 Walker 256 癌肉瘤的生长动态。在导致下丘脑性尿崩症的加压素基因突变的 Brattleboro 大鼠中被检测到。WAG 大鼠是正常加压素基因的携带者。另一个连锁的等位基因差异与控制黑色素合成的酪氨酸酶基因有关。WAG 大鼠表达的突变等位基因决定了白化表型。Brattleboro 大鼠有正常工作的酪氨酸酶基因。F2 分离产生了具有两种肿瘤生长模式的表型类群:线性生长或退化。肿瘤退化与酪氨酸酶活性无关,仅在尿崩症大鼠中观察到。对 F3 和 F4 代突变体的分析证实了 Walker 256 癌肉瘤生长模式的这种规律性。

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