Wobus U, Bäumlein H, Panitz R, Serfling E, Kafatos F C
Cell. 1980 Nov;22(1 Pt 1):127-35. doi: 10.1016/0092-8674(80)90161-0.
The Balbiani ring (BR) DNAs show prominent periodicities of restriction enzyme sites. Studies using a cloned fragment of the BRc gene strongly suggest that these periodicities reflect the existence of tandemly repetitive sequences within BR DNA. Tandem repeats measuring 54-58 bp have been demonstrated by partial sequence analysis of the BRc clone; the restriction site periodicities suggest the existence of additional 175 (= 3 X 58) and 1050 (= 6 X 175) bp repeat units. The short, medium and long repeats (58, 175 and 1050 bp, respectively) show sequence homology. Constrained unequal crossing over (resulting from misalignment of repeat arrays, usually by one repeat) is proposed as the mechanism for evolution of short, medium and long repeats from each other, in a manner analogous to evolution of satellite DNA sequences. Paradoxically, the dominant restriction site periodicities appear to be more conservative than might be expected on the basis of the overall sequence divergence between the sequenced repeats. This may be a consequence of functionally important, long-range amino acid or oligopeptide periodicities (for example, Asp x Ser or Glu x Ser corresponding to Hinf I sites) in the BRc protein product, in conjunction with preferential use of certain synonymous codons.
巴尔比亚尼环(BR)DNA显示出明显的限制性酶切位点周期性。使用BRc基因的克隆片段进行的研究强烈表明,这些周期性反映了BR DNA中串联重复序列的存在。通过对BRc克隆的部分序列分析,已证实存在长度为54 - 58 bp的串联重复序列;限制性酶切位点的周期性表明还存在额外的175(= 3×58)和1050(= 6×175)bp重复单元。短、中、长重复序列(分别为58、175和1050 bp)显示出序列同源性。提出受限的不等交换(通常由重复阵列的错配导致,一般相差一个重复序列)是短、中、长重复序列相互演化的机制,其方式类似于卫星DNA序列的演化。矛盾的是,主要的限制性酶切位点周期性似乎比根据已测序重复序列之间的总体序列差异所预期的更为保守。这可能是由于BRc蛋白产物中功能重要的长程氨基酸或寡肽周期性(例如,对应于Hinf I位点的Asp x Ser或Glu x Ser),以及某些同义密码子的优先使用所致。