Luengo Hendriks Cris L, Keränen Soile V E, Fowlkes Charless C, Simirenko Lisa, Weber Gunther H, DePace Angela H, Henriquez Clara, Kaszuba David W, Hamann Bernd, Eisen Michael B, Malik Jitendra, Sudar Damir, Biggin Mark D, Knowles David W
Berkeley Drosophila Transcription Network Project, Life Sciences Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, Berkeley, CA 94720, USA.
Genome Biol. 2006;7(12):R123. doi: 10.1186/gb-2006-7-12-r123.
To model and thoroughly understand animal transcription networks, it is essential to derive accurate spatial and temporal descriptions of developing gene expression patterns with cellular resolution.
Here we describe a suite of methods that provide the first quantitative three-dimensional description of gene expression and morphology at cellular resolution in whole embryos. A database containing information derived from 1,282 embryos is released that describes the mRNA expression of 22 genes at multiple time points in the Drosophila blastoderm. We demonstrate that our methods are sufficiently accurate to detect previously undescribed features of morphology and gene expression. The cellular blastoderm is shown to have an intricate morphology of nuclear density patterns and apical/basal displacements that correlate with later well-known morphological features. Pair rule gene expression stripes, generally considered to specify patterning only along the anterior/posterior body axis, are shown to have complex changes in stripe location, stripe curvature, and expression level along the dorsal/ventral axis. Pair rule genes are also found to not always maintain the same register to each other.
The application of these quantitative methods to other developmental systems will likely reveal many other previously unknown features and provide a more rigorous understanding of developmental regulatory networks.
为了构建和深入理解动物转录网络,以细胞分辨率获得发育中基因表达模式的准确时空描述至关重要。
在此,我们描述了一套方法,这些方法首次以细胞分辨率对整个胚胎中的基因表达和形态进行了定量三维描述。发布了一个包含来自1282个胚胎信息的数据库,该数据库描述了果蝇胚盘在多个时间点的22个基因的mRNA表达。我们证明我们的方法足够准确,能够检测到以前未描述的形态和基因表达特征。细胞胚盘显示出具有复杂的核密度模式形态以及与后期著名形态特征相关的顶/基位移。成对规则基因表达条纹通常被认为仅沿前后体轴指定模式,但研究表明其在沿背/腹轴的条纹位置、条纹曲率和表达水平上具有复杂变化。还发现成对规则基因彼此之间并不总是保持相同的对齐方式。
将这些定量方法应用于其他发育系统可能会揭示许多其他以前未知的特征,并对发育调控网络提供更严谨的理解。