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修饰小鼠主要尿蛋白表达的基因。

Genes that modify expression of major urinary proteins in mice.

作者信息

Duncan R, Matthai R, Huppi K, Roderick T, Potter M

机构信息

Laboratory of Genetics, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

Mol Cell Biol. 1988 Jul;8(7):2705-12. doi: 10.1128/mcb.8.7.2705-2712.1988.

Abstract

A survey of major urinary proteins (MUPs) from eight BALB/c mouse substrains by isoelectric focusing identified a common pattern with about 10 protein bands in males. One substrain, BALB/cJPt, differed in that it expressed two variant MUP patterns, designated 4.1lo and null. To find the chromosomal location of the gene which determines the 4.1lo phenotype, BALB/cJPt-MUP-4.1lo was crossed with a wild-derived Mus musculus domesticus inbred strain (CLA) that expresses the common BALB/c MUP pattern. The F1 phenotype revealed that the gene(s) controlling the MUP-4.1lo trait was recessive. A restriction fragment polymorphism between these strains found with a MUP cDNA probe allowed us to establish that a gene determining the MUP-4.1lo trait was not linked to the MUP structural genes on chromosome 4. Assays for other chromosomal marker loci revealed that a gene determining the MUP-4.1lo trait, designated Mupm-1, was closely linked to Myc-1 on chromosome 15. To determine the genetic basis of the null trait, BALB/cJPt-MUP-null mice were crossed with BALB/cJPt-MUP-4.1lo mice. A MUP restriction fragment polymorphism between these two lines was tightly linked to a gene or genes involved in determining the MUP-null phenotype. The two variant MUP phenotypes in BALB/cJ mice are determined by separate genes, one of which is located on chromosome 4 and the other on chromosome 15. The chromosomal location of Mupm-1 suggests that it produces a trans-acting factor which regulates MUP expression.

摘要

通过等电聚焦对八个BALB/c小鼠亚系的主要尿蛋白(MUPs)进行调查,发现雄性小鼠中有一个约10条蛋白带的常见模式。一个亚系BALB/cJPt有所不同,它表达两种变异的MUP模式,分别命名为4.1lo和无。为了找到决定4.1lo表型的基因的染色体定位,将BALB/cJPt-MUP-4.1lo与表达常见BALB/c MUP模式的野生来源小家鼠近交系(CLA)进行杂交。F1表型显示,控制MUP-4.1lo性状的基因是隐性的。用MUP cDNA探针在这些品系之间发现的限制性片段多态性使我们能够确定,决定MUP-4.1lo性状的基因与4号染色体上的MUP结构基因不连锁。对其他染色体标记位点的检测表明,决定MUP-4.1lo性状的基因(命名为Mupm-1)与15号染色体上的Myc-1紧密连锁。为了确定无性状的遗传基础,将BALB/cJPt-MUP-无小鼠与BALB/cJPt-MUP-4.1lo小鼠进行杂交。这两个品系之间的MUP限制性片段多态性与一个或多个参与决定MUP无表型的基因紧密连锁。BALB/cJ小鼠中的两种变异MUP表型由不同的基因决定,其中一个位于4号染色体上,另一个位于15号染色体上。Mupm-1的染色体定位表明它产生一种反式作用因子,调节MUP的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/247d/363481/6b8beccb707b/molcellb00067-0040-a.jpg

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