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通过向晚期幼虫注射吗啉代寡核苷酸来操纵紫海胆(强壮紫海胆)发育中的幼体结构。

Manipulation of developing juvenile structures in purple sea urchins (Strongylocentrotus purpuratus) by morpholino injection into late stage larvae.

作者信息

Heyland Andreas, Hodin Jason, Bishop Cory

机构信息

Integrative Biology, University of Guelph, Guelph, Ontario, Canada.

Hopkins Marine Station, Stanford University, Pacific Grove, CA, United States of America.

出版信息

PLoS One. 2014 Dec 1;9(12):e113866. doi: 10.1371/journal.pone.0113866. eCollection 2014.

Abstract

Sea urchins have been used as experimental organisms for developmental biology for over a century. Yet, as is the case for many other marine invertebrates, understanding the development of the juveniles and adults has lagged far behind that of their embryos and larvae. The reasons for this are, in large part, due to the difficulty of experimentally manipulating juvenile development. Here we develop and validate a technique for injecting compounds into juvenile rudiments of the purple sea urchin, Strongylocentrotus purpuratus. We first document the distribution of rhodaminated dextran injected into different compartments of the juvenile rudiment of sea urchin larvae. Then, to test the potential of this technique to manipulate development, we injected Vivo-Morpholinos (vMOs) designed to knock down p58b and p16, two proteins involved in the elongation of S. purpuratus larval skeleton. Rudiments injected with these vMOs showed a delay in the growth of some juvenile skeletal elements relative to controls. These data provide the first evidence that vMOs, which are designed to cross cell membranes, can be used to transiently manipulate gene function in later developmental stages in sea urchins. We therefore propose that injection of vMOs into juvenile rudiments, as shown here, is a viable approach to testing hypotheses about gene function during development, including metamorphosis.

摘要

一个多世纪以来,海胆一直被用作发育生物学的实验生物。然而,与许多其他海洋无脊椎动物一样,对幼体和成体发育的了解远远落后于对其胚胎和幼虫的了解。造成这种情况的主要原因是对幼体发育进行实验操作存在困难。在此,我们开发并验证了一种将化合物注入紫海胆(Strongylocentrotus purpuratus)幼体原基的技术。我们首先记录了注入海胆幼虫幼体原基不同区域的罗丹明标记葡聚糖的分布情况。然后,为了测试该技术对发育进行操作的潜力,我们注入了旨在敲低p58b和p16的活体吗啉代寡核苷酸(vMOs),这两种蛋白质参与紫海胆幼虫骨骼的伸长。与对照组相比,注入这些vMOs的原基显示出一些幼体骨骼元素的生长延迟。这些数据首次证明,旨在穿过细胞膜的vMOs可用于在海胆发育后期短暂操纵基因功能。因此,我们提出,如本文所示,将vMOs注入幼体原基是一种可行的方法,可用于检验有关发育过程中基因功能的假设,包括变态发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55fa/4250057/6db416f09c3f/pone.0113866.g001.jpg

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