A set of 1,378 expressed sequence tags (ESTs), both the 5'-most and T-most
ends, derived from Ciona intestinalis fertilized eggs was categorized into
1,003 independent clusters. When compared with sequences in databases, 452
of the clusters showed significant matches with reported proteins, while 19
0 showed matches with putative proteins for which there is not enough infor
mation to categorize their function, and 361 had no significant similaritie
s to known proteins. Sequence similarity analyses of the 452 clusters in re
lation to the biological function as well as the structure of the message p
opulation at this stage demonstrated that 362 of them have functions that m
any kinds of cells use, 65 are associated with cell-cell communication, inc
luding a candidate cDNA for sonic hedgehog, and 25 are transcription factor
s. Sequence prevalence distribution analysis demonstrated that the great ma
jority (78%) of the mRNAs are rare mRNAs or are represented by a single clo
ne/cluster. All of the 1,003 clusters were subjected to whole-mount in situ
hybridization to analyze the distribution of the maternal mRNAs in fertili
zed eggs, and a total of 329 genes showed localized distribution of the mRN
As: 16 showed cortical localization, 12 showed mitochondrial-like distribut
ion, 99 crescent-like distribution, 63 partial localization, and 139 weak l
ocalization. When the distribution pattern of all the maternally expressed
mRNAs was examined in the 8-cell stage embryos, it became evident that 248
genes which have localized mRNA patterns at the fertilized egg stage lose t
heir localized distribution by the 8-cell stage. In contrast, 13 genes newl
y gain a localized pattern by the 8-cell stage. In addition, a total of 39
genes showed distinct in situ signals in the nucleus of blastomeres of the
8-cell stage embryo, suggesting early zygotic expression of these genes by
this stage. These results suggest that complicated cytoplasmic movements ar
e associated with the characteristic distribution of maternal mRNAs, which
in turn support proper embryonic axis formation and establishment of the ge
netic network for embryonic cell specification. (C) 2001 Academic Press.