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Integrative Analysis of Three RNA Sequencing Methods Identifies Mutually Exclusive Exons of MADS-Box Isoforms During Early Bud Development in Picea abies

机译:三种RNA测序方法的综合分析确定了青海云杉早期芽发育过程中MADS-Box亚型的互斥外显子。

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摘要

Recent efforts to sequence the genomes and transcriptomes of several gymnosperm species have revealed an increased complexity in certain gene families in gymnosperms as compared to angiosperms. One example of this is the gymnosperm sister clade to angiosperm TM3-like MADS-box genes, which at least in the conifer lineage has expanded in number of genes. We have previously identified a member of this sub-clade, the conifer gene DEFICIENS AGAMOUS LIKE 19 (DAL19), as being specifically upregulated in cone-setting shoots. Here, we show through Sanger sequencing of mRNA-derived cDNA and mapping to assembled conifer genomic sequences that DAL19 produces six mature mRNA splice variants in Picea abies. These splice variants use alternate first and last exons, while their four central exons constitute a core region present in all six transcripts. Thus, they are likely to be transcript isoforms. Quantitative Real-Time PCR revealed that two mutually exclusive first DAL19 exons are differentially expressed across meristems that will form either male or female cones, or vegetative shoots. Furthermore, mRNA in situ hybridization revealed that two mutually exclusive last DAL19 exons were expressed in a cell-specific pattern within bud meristems. Based on these findings in DAL19, we developed a sensitive approach to transcript isoform assembly from short-read sequencing of mRNA. We applied this method to 42 putative MADS-box core regions in P. abies, from which we assembled 1084 putative transcripts. We manually curated these transcripts to arrive at 933 assembled transcript isoforms of 38 putative MADS-box genes. 152 of these isoforms, which we assign to 28 putative MADS-box genes, were differentially expressed across eight female, male, and vegetative buds. We further provide evidence of the expression of 16 out of the 38 putative MADS-box genes by mapping PacBio Iso-Seq circular consensus reads derived from pooled sample sequencing to assembled transcripts. In summary, our analyses reveal the use of mutually exclusive exons of MADS-box gene isoforms during early bud development in P. abies, and we find that the large number of identified MADS-box transcripts in P. abies results not only from expansion of the gene family through gene duplication events but also from the generation of numerous splice variants.
机译:最近对几种裸子植物物种的基因组和转录组测序的努力表明,与裸子植物相比,裸子植物某些基因家族的复杂性增加。一个例子是裸子植物姐妹进化枝到被子植物TM3样的MADS-box基因,至少在针叶树系中它的基因数目已经扩大。我们先前已经确定了该子类中的一个成员,即针叶树基因DEFICIENS AGAMOUS LIKE 19(DAL19),在定锥芽中被特别上调了。在这里,我们通过Sanger测序从mRNA衍生的cDNA进行测序,并映射到组装的针叶树基因组序列,DAL19在云杉中产生了六个成熟的mRNA剪接变体。这些剪接变体使用交替的第一个和最后一个外显子,而它们的四个中央外显子构成了所有六个转录本中存在的核心区域。因此,它们很可能是转录亚型。实时定量PCR分析显示,两个互斥的首个DAL19外显子在分生组织中差异表达,这些分生组织将形成雄性或雌性视锥细胞或营养枝。此外,mRNA原位杂交显示两个互斥的最后DAL19外显子在芽分生组织内以细胞特异性模式表达。基于DAL19中的这些发现,我们开发了一种敏感的方法,可通过mRNA的短读测序实现转录亚型装配。我们将这种方法应用到了假单胞菌的42个假定的MADS-box核心区域,从中我们组装了1084个假定的转录本。我们手动策划这些成绩单,以获得38个假定的MADS-box基因的933个组装成绩单亚型。这些同工型中的152个(我们分配给28个假定的MADS-box基因)在8个雌性,雄性和植物性芽中差异表达。通过将来自合并样品测序的PacBio Iso-Seq环状共有序列读图映射到组装的转录本,我们进一步提供了38个推定的MADS-box基因中16个表达的证据。总而言之,我们的分析揭示了在假单胞菌早期芽发育过程中,MADS-box基因同工型互斥的外显子的使用,并且我们发现,在假单胞菌中,大量已鉴定的MADS-box转录物不仅是由于扩大了基因家族通过基因复制事件产生,也来自众多剪接变体的产生。

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