Baier L J, Hanash S M, Erickson R P
Proc Natl Acad Sci U S A. 1984 Apr;81(7):2132-6. doi: 10.1073/pnas.81.7.2132.
Radiation-induced chromosomal deletions involving the albino locus region of the mouse result, when homozygous, in abnormalities ranging from sterility to lethality at various stages of development. We have utilized two-dimensional electrophoresis to search for polypeptide alterations in livers from newborn mice homozygous for the c14CoS and c3H deletions and also from c3H/c6H compound heterozygote mice. Five-hundred polypeptide spots detectable in normal mouse liver gels were scored. Alterations involving five polypeptides were observed in the various overlapping deletions. A spot corresponding to a polypeptide with a 38,000 Mr was missing from mice homozygous for the short c14CoS and the longer overlapping c3H deletions. Another polypeptide with a 29,000 Mr was missing from c3H homozygotes and c3H/c6H heterozygotes. A third polypeptide with a 62,000 Mr was missing only from c3H homozygotes. Two additional polypeptides were markedly increased in amount in c14CoS and c3H homozygotes. The partial overlap between the three deletions analyzed allows provisional genetic mapping of previously unknown loci for three of the five electrophoretically identifiable polypeptides expressed in newborn mouse livers. The results obtained provide a basis for studying radiation-induced deletions with two-dimensional electrophoresis gels.
辐射诱导的涉及小鼠白化病基因座区域的染色体缺失,当纯合时,会导致从发育的各个阶段的不育到致死等各种异常情况。我们利用二维电泳来寻找纯合的c14CoS和c3H缺失的新生小鼠肝脏以及c3H/c6H复合杂合子小鼠肝脏中的多肽变化。对正常小鼠肝脏凝胶中可检测到的500个多肽斑点进行了评分。在各种重叠缺失中观察到涉及五种多肽的变化。对于纯合的短c14CoS和较长的重叠c3H缺失的小鼠,对应于分子量为38,000的多肽的一个斑点缺失。c3H纯合子和c3H/c6H杂合子中缺失了另一个分子量为29,000的多肽。仅在c3H纯合子中缺失了第三个分子量为62,000的多肽。另外两种多肽在c14CoS和c3H纯合子中的含量明显增加。对分析的三个缺失之间的部分重叠使得能够对新生小鼠肝脏中表达的五种电泳可识别多肽中的三种进行先前未知基因座的初步遗传定位。所获得的结果为利用二维电泳凝胶研究辐射诱导的缺失提供了基础。