Jacobson M
J Neurosci. 1981 Aug;1(8):918-22. doi: 10.1523/JNEUROSCI.01-08-00918.1981.
Clonal origins of Rohon-Beard neurons in Xenopus were determined quantitatively by injecting horseradish peroxidase into individual blastomeres at the 16-cell stage and later counting labeled and unlabeled Rohon-Beard neurons. Two different patterns of cleavage were selected. In pattern X, all Rohon-Beard neurons originated from three blastomeres (V1.1, V1.2, and V2.2) on each side; in pattern Y, all Rohon Beard neurons originated from two blastomeres (V1.2 and V2.2) on each side. Counts of Rohon-Beard neurons at larval stages 32 to 34 showed that 96 to 100% (mean 99%) originated from blastomeres on the same side; of these, 68 to 90% (mean 75%) descended from V1.2, 20 to 31% (mean 24%) descended from V2.2, 0 to 7% descended from V1.1. The significance of the regionally restricted origin of Rohon-Beard neurons is discussed.
通过在16细胞期向单个卵裂球注射辣根过氧化物酶,然后对标记和未标记的罗霍恩 - 比尔兹神经元进行计数,定量确定了非洲爪蟾中罗霍恩 - 比尔兹神经元的克隆起源。选择了两种不同的卵裂模式。在模式X中,所有罗霍恩 - 比尔兹神经元均起源于每侧的三个卵裂球(V1.1、V1.2和V2.2);在模式Y中,所有罗霍恩 - 比尔兹神经元均起源于每侧的两个卵裂球(V1.2和V2.2)。对第32至34期幼虫阶段的罗霍恩 - 比尔兹神经元计数表明,96%至100%(平均99%)起源于同侧的卵裂球;其中,68%至90%(平均75%)来自V1.2,20%至31%(平均24%)来自V2.2,0%至7%来自V1.1。讨论了罗霍恩 - 比尔兹神经元区域受限起源的意义。