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牛和小鼠尿路上皮膜蛋白基因的染色体定位

Chromosomal localization of uroplakin genes of cattle and mice.

作者信息

Ryan A M, Womack J E, Yu J, Lin J H, Wu X R, Sun T T, Clarke V, D'Eustachio P

机构信息

Department of Veterinary Pathobiology, Texas A&M University, College Station 77843.

出版信息

Mamm Genome. 1993 Nov;4(11):656-61. doi: 10.1007/BF00360903.

Abstract

The asymmetric unit membrane (AUM) of the apical surface of mammalian urinary bladder epithelium contains several major integral membrane proteins, including uroplakins IA and IB (both 27 kDa), II (15 kDa), and III (47 kDa). These proteins are synthesized only in terminally differentiated bladder epithelial cells. They are encoded by separate genes and, except for uroplakins IA and IB, appear to be unrelated in their amino acid sequences. The genes encoding these uroplakins were mapped to chromosomes of cattle through their segregation in a panel of bovine x rodent somatic cell hybrids. Genes for uroplakins IA, IB, and II were mapped to bovine (BTA) Chromosomes (Chrs) 18 (UPK1A), 1 (UPK1B), and 15 (UPK2), respectively. Two bovine genomic DNA sequences reactive with a uroplakin III cDNA probe were identified and mapped to BTA 6 (UPK3A) and 5 (UPK3B). We have also mapped genes for uroplakins IA and II in mice, to the proximal regions of mouse Chr 7 (Upk1a) and 9 (Upk2), respectively, by analyzing the inheritance of restriction fragment length variants in recombinant inbred mouse strains. These assignments are consistent with linkage relationships known to be conserved between cattle and mice. The mouse genes for uroplakins IB and III were not mapped because the mouse genomic DNA fragments reactive with each probe were invariant among the inbred strains tested. Although the stoichiometry of AUM proteins is nearly constant, the fact that the uroplakin genes are unlinked indicates that their expression must be independently regulated. Our results also suggest likely positions for two human uroplakin genes and should facilitate further analysis of their possible involvement in disease.

摘要

哺乳动物膀胱上皮细胞顶端表面的不对称单位膜(AUM)含有几种主要的整合膜蛋白,包括尿血小板溶素IA和IB(均为27 kDa)、II(15 kDa)和III(47 kDa)。这些蛋白仅在终末分化的膀胱上皮细胞中合成。它们由不同的基因编码,除尿血小板溶素IA和IB外,其氨基酸序列似乎没有关联。通过在一组牛×啮齿动物体细胞杂种中的分离,将编码这些尿血小板溶素的基因定位到牛的染色体上。尿血小板溶素IA、IB和II的基因分别定位到牛(BTA)染色体(Chrs)18(UPK1A)、1(UPK1B)和15(UPK2)上。鉴定出两个与尿血小板溶素III cDNA探针反应的牛基因组DNA序列,并将其定位到BTA 6(UPK3A)和5(UPK3B)上。通过分析重组近交小鼠品系中限制性片段长度变异的遗传情况,我们还将小鼠中的尿血小板溶素IA和II基因分别定位到小鼠Chr 7(Upk1a)和9(Upk2)的近端区域。这些定位与已知在牛和小鼠之间保守的连锁关系一致。未定位小鼠中尿血小板溶素IB和III的基因,因为与每个探针反应的小鼠基因组DNA片段在测试的近交品系中是不变的。尽管AUM蛋白的化学计量几乎恒定,但尿血小板溶素基因不连锁这一事实表明它们的表达必须受到独立调控。我们的结果还提示了两个人类尿血小板溶素基因的可能位置,并应有助于进一步分析它们可能与疾病的关联。

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