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小鼠心房利钠因子基因的定位。与Fv-1基因座紧密连锁的证据。

Mapping of the mouse atrial natriuretic factor gene. Evidence for tight linkage to the Fv-1 locus.

作者信息

Mullins J J, Zeng Q, Gross K W

出版信息

Hypertension. 1987 May;9(5):518-21. doi: 10.1161/01.hyp.9.5.518.

Abstract

The importance of atrial natriuretic factor (ANF) in the regulation of salt balance and blood pressure is now widely recognized, and it would be extremely informative for both physiologists and molecular biologists to have mutants available that exhibit abnormal expression of this peptide hormone. The most direct mutation would affect the structural gene itself by altering either its coding potential or its regulation. With this aim in mind, it is of considerable interest to accurately determine the chromosomal position of the ANF gene (Anf) in the mouse. This information would permit a comparison with known mutations and provide a means of screening for mutations at this locus. Using recombinant inbred mouse strains, we undertook the mapping of the mouse Anf gene and demonstrated linkage of the gene to the Friend virus susceptibility-1 (Fv-1) locus on chromosome 4. The mapping was performed using a restriction fragment length polymorphism extant between the two parental strains. No recombination event between Anf and the Fv-1 locus was evident in any of the 34 strains tested. The assignment of Anf to this region of chromosome 4 coincides with the reported position of the cribriform degeneration mutation, which includes in its phenotype an abnormal electrolyte distribution. We have, therefore, begun studying this mutation to determine whether a defect in ANF expression is the underlying cause of the phenotype. Thus far, we have found no major DNA rearrangement close to the Anf gene.

摘要

心房利钠因子(ANF)在盐平衡和血压调节中的重要性现已得到广泛认可,对于生理学家和分子生物学家而言,拥有表现出这种肽类激素异常表达的突变体将极具参考价值。最直接的突变会通过改变其编码潜能或调节方式来影响结构基因本身。出于这一目的,准确确定小鼠中ANF基因(Anf)的染色体位置就显得相当有趣。这一信息将有助于与已知突变进行比较,并提供一种筛选该位点突变的方法。利用重组近交系小鼠品系,我们对小鼠Anf基因进行了定位,并证明该基因与4号染色体上的Friend病毒易感性-1(Fv-1)位点连锁。定位是利用两个亲本品系之间存在的限制性片段长度多态性进行的。在测试的34个品系中,Anf与Fv-1位点之间均未出现重组事件。将Anf定位于4号染色体的这一区域,与筛状变性突变的报道位置相符,该突变的表型包括异常的电解质分布。因此,我们已开始研究这一突变,以确定ANF表达缺陷是否是该表型的根本原因。到目前为止,我们尚未在Anf基因附近发现重大的DNA重排。

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