USDA-ARS, Southern Regional Research Center, Cotton Fiber Bioscience, 1100 Robert E. Lee Blvd, New Orleans, LA 70124 USA.
Gene. 2012 Feb 25;494(2):181-9. doi: 10.1016/j.gene.2011.12.018. Epub 2011 Dec 20.
Cellulose synthase catalytic subunits (CesAs) are the catalytic sites within a multisubunit complex for cellulose biosynthesis in plants. CesAs have been extensively studied in diploid plants, but are not well characterized in polyploid plants. Gossypium hirsutum is an allotetraploid cotton species producing over 90% of the world's cotton fibers. Although G. hirsutum CesAs (GhCesAs) are responsible for cellulose production in cotton fiber, very limited numbers of GhCesA genes have been identified. Here, we report isolating and characterizing a pair of homeologous CesA2 genes and their full-length cDNAs from allotetraploid cotton. The GhCesA2-A(T) gene from the A-subgenome and GhCesA2-D(T) gene from the D-subgenome were screened from a G. hirsutum BAC library. These genes shared 92% sequence similarity throughout the entire sequence. The coding sequences were nearly identical, and the deduced amino acid sequences from GhCesA2-A(T) (1,039 amino acids) and GhCesA2-D(T) (1,040 amino acids) were identical except four amino acids, whereas the noncoding sequences showed divergence. Sequence analyses showed that all exons of GhCesA2-A(T) contained consensus splice donor dinucleotides, but one exon in GhCesA2-D(T) contained nonconsensus splice donor dinucleotides. Although the nonconsensus splice donor dinucleotides were previously suggested to be involved in alternative splice or pseudogenization, our results showed that a majority of GhCesA2-A(T) and GhCesA2-D(T) transcripts consisted of functional and full-length transcripts with little evidence for alternative mRNA isoforms in developing cotton fibers. Expression analyses showed that GhCesA2-A(T) and GhCesA2-D(T) shared common temporal and spatial expression patterns, and they were highly and preferentially expressed during the cellulose biosynthesis stage in developing cotton fibers. The observations of higher expression levels of both GhCesA2-A(T) and GhCesA2-D(T) in developing fibers of one near-isogenic line (NIL) with higher fiber bundle strength over the other NIL with lower fiber bundle strength suggested that the differential expression of genes associated with secondary cell wall cellulose biosynthesis in developing fiber might affect cotton fiber properties.
纤维素合酶催化亚基(CesAs)是植物纤维素生物合成多亚基复合物中的催化位点。CesAs 在二倍体植物中得到了广泛研究,但在多倍体植物中尚未得到很好的表征。陆地棉是一种异源四倍体棉种,生产了世界上 90%以上的棉花纤维。尽管陆地棉 CesAs(GhCesAs)负责棉花纤维的纤维素生产,但已鉴定的 GhCesA 基因数量非常有限。在这里,我们报告了从异源四倍体棉中分离和鉴定一对同源 CesA2 基因及其全长 cDNA。从陆地棉 BAC 文库中筛选出 A 亚基因组的 GhCesA2-A(T)基因和 D 亚基因组的 GhCesA2-D(T)基因。这些基因在整个序列中具有 92%的序列相似性。编码序列几乎完全相同,从 GhCesA2-A(T)(1039 个氨基酸)和 GhCesA2-D(T)(1040 个氨基酸)推导的氨基酸序列除了四个氨基酸外完全相同,而非编码序列则存在差异。序列分析表明,GhCesA2-A(T)的所有外显子都包含保守的剪接供体二核苷酸,但 GhCesA2-D(T)的一个外显子含有非保守的剪接供体二核苷酸。尽管以前曾提出非保守的剪接供体二核苷酸参与可变剪接或假基因化,但我们的结果表明,大多数 GhCesA2-A(T)和 GhCesA2-D(T)转录物由功能齐全的全长转录物组成,在发育中的棉花纤维中几乎没有证据表明存在可变 mRNA 异构体。表达分析表明,GhCesA2-A(T)和 GhCesA2-D(T)具有共同的时空表达模式,在发育中的棉花纤维纤维素生物合成阶段高度且优先表达。在一个近等基因系(NIL)中,GhCesA2-A(T)和 GhCesA2-D(T)的表达水平均较高,纤维束强度高于另一个 NIL,这表明与次生细胞壁纤维素生物合成相关的基因在发育中的纤维中的差异表达可能影响棉花纤维的性质。