Flavell R A, Kooter J M, De Boer E, Little P F, Williamson R
Cell. 1978 Sep;15(1):25-41. doi: 10.1016/0092-8674(78)90080-6.
Total human DNA was cleaved with a variety of restriction enzymes, and the fragments were fractionated by gel electrophoresis and transferred to nitrocellulose filter strips. The restricted DNA was then hybridized to nick-translated radioactive recombinant plasmid DNA containing sequences derived from human beta-globin messenger RNA. Under suitable conditions, this probe hybridizes with both the beta--and delta-globin genes. Using this probe, a restriction map of the human beta--and delta-globin genes and the surrounding genomic DNA regions has been constructed. The beta-globin gene contains a nonglobin DNA insert approximately 899-1000 base pairs in length, present within the sequence coding for amino acids 101-120 of the 146 amino acid long globin polypeptide. A similar sequence may be present within the same sequence of the delta-globin gene. The distance between the beta--and delta-globin genes is approximately 7000 nucleotide pairs, and the delta-globin gene is to the 5' side of the beta-globin gene, as predicted by genetic evidence. Both genes are transcribed from the same DNA strand. The structure of the Hb Lepore gene is shown to be a fused delta--and beta-globin gene, and to be completely consistent with the derived map of normal beta--and delta-globin genes. [Restriction enzyme nomenclature follows that of Smith and Nathans (1973) and Roberts (1976). A genomic DNA restriction fragment containing part or all of one globin gene will be designated by that globin chain--for instance, the Pst I fragment containing the beta-globin gene sequence will be designated Pst I beta. A similar convention will be used for double digests. Throughout this paper, when reference is made to the 5' or 3' side or fragment of a gene, this refers to the 5' or 3' side of the mRNA coded by that sequence. Thus the 5' side (N terminal) of the beta-globulin gene is the sequence to the 5' side of the anti-sense strand.].
用人的总DNA与多种限制性内切酶进行切割,片段经凝胶电泳分离后转移至硝酸纤维素滤纸条上。然后将限制性内切酶切割后的DNA与经切口平移法标记的放射性重组质粒DNA杂交,该重组质粒DNA含有源自人β-珠蛋白信使RNA的序列。在合适的条件下,该探针可与β-珠蛋白基因和δ-珠蛋白基因杂交。利用该探针构建了人β-珠蛋白基因和δ-珠蛋白基因以及周围基因组DNA区域的限制性图谱。β-珠蛋白基因含有一个长度约为899 - 1000个碱基对的非珠蛋白DNA插入片段,位于由146个氨基酸组成的珠蛋白多肽第101 - 120位氨基酸编码序列内。δ-珠蛋白基因的相同序列中可能也存在类似序列。β-珠蛋白基因和δ-珠蛋白基因之间的距离约为7000个核苷酸对,正如遗传学证据所预测的,δ-珠蛋白基因位于β-珠蛋白基因的5′端一侧。两个基因都从同一条DNA链转录。Hb Lepore基因的结构显示为一个融合的δ-珠蛋白基因和β-珠蛋白基因,与正常β-珠蛋白基因和δ-珠蛋白基因的推导图谱完全一致。[限制性内切酶命名遵循Smith和Nathans(1973年)以及Roberts(1976年)的命名法。包含一个珠蛋白基因部分或全部的基因组DNA限制性片段将由该珠蛋白链命名——例如,含有β-珠蛋白基因序列的Pst I片段将命名为Pst I β。双酶切采用类似的命名法。在本文中,当提及基因的5′端或3′端或片段时,指的是由该序列编码的mRNA的5′端或3′端。因此,β-球蛋白基因的5′端(N端)是反义链5′端的序列。]