Brun C, Jullien N, Jacobzone M, Gautier C, Miassod R
Laboratoire de Génétique et Physiologie du Développement, Parc Scientifique de Luminy, Marseille, France.
Exp Cell Res. 1995 Oct;220(2):338-47. doi: 10.1006/excr.1995.1324.
In Drosophila, sequences anchoring the DNA molecule to the scaffold (SARs) and sequences able to replicate autonomously (ARSs) had been shown to comap on an 835-kb DNA fragment (Brun et al. (1990) Mol. Cell. Biol. 10, 5455-5463). To investigate the question of whether this comapping results from the coincidental recruitment of SARs and ARSs in A,T-rich regions, A,T-rich regions of the 835-kb DNA fragment have been identified by restriction analysis with enzymes recognizing motifs made exclusively of A and T. Within the limits of sensitivity of this approach, the obtained data favor the idea of a noncoincidental recruitment: obviously a SAR and an ARS subpopulation are preferentially localized in the A,T-rich regions, but not every A,T-rich region displays a SAR activity, or an ARS activity, or both, nor are all SARs or ARSs localized in the A,T-rich regions. In addition, the data support the idea that a statistical assessment of base composition using restriction analysis might be developed into a general useful approach to genome organization.
在果蝇中,将DNA分子锚定到支架上的序列(SARs)和能够自主复制的序列(ARSs)已被证明在一个835 kb的DNA片段上共定位(Brun等人,(1990年)《分子与细胞生物学》10,5455 - 5463)。为了研究这种共定位是否是由于SARs和ARSs在富含A、T的区域偶然募集所致,通过用识别仅由A和T组成的基序的酶进行限制性分析,已鉴定出835 kb DNA片段的富含A、T的区域。在这种方法的灵敏度范围内,所获得的数据支持非偶然募集的观点:显然,一个SAR亚群和一个ARS亚群优先定位于富含A、T的区域,但并非每个富含A、T的区域都显示出SAR活性或ARS活性,或两者兼具,也并非所有的SARs或ARSs都定位于富含A、T的区域。此外,数据支持这样一种观点,即利用限制性分析对碱基组成进行统计评估可能会发展成为一种研究基因组组织的通用有效方法。