ClPS1 gene-mediated manipulation of 2n pollen formation enables the creation of triploid seedless watermelon.

IF 8.1 Q1 HORTICULTURE
Wenyu Pang, Qiaran Wang, Chenxin Li, Wenbing He, Jiafa Wang, Shujuan Tian, Li Yuan
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引用次数: 0

Abstract

Seedless watermelons are increasingly dominating the consumer market due to their convenience and high quality. However, traditional triploid watermelon breeding faces challenges such as long breeding cycles and low survival rates of triploid F1 progeny, severely hindering both breeding and production. In this study, we identified the ClPS1 gene as being associated with the formation of 2n gametes in watermelon. Expression analysis revealed that ClPS1 is highly expressed during meiosis and microsporogenesis. Using CRISPR/Cas9, we generated ClPS1-targeted mutants, which disrupted chromosome segregation at metaphase II. This led to the production of diploid male spores and abnormal division of male spores, ultimately generating diploid pollen grains, while female meiosis remained unaffected. Moreover, self-fertilization or crosses using these mutants as paternal parents yielded triploid and aneuploid watermelons. Our findings demonstrate, for the first time, the molecular manipulation of 2n gametes to create triploid seedless watermelons, offering new insights into polyploid breeding and evolutionary studies in the Cucurbitaceae family and other species.

ClPS1基因介导的2n花粉形成调控可以产生三倍体无籽西瓜。
无籽西瓜因其方便和高品质而日益主导着消费市场。然而,传统的三倍体西瓜育种面临育种周期长、三倍体F1后代成活率低等挑战,严重阻碍了西瓜的育种和生产。在本研究中,我们发现ClPS1基因与西瓜2n个配子的形成有关。表达分析表明,ClPS1在减数分裂和小孢子发生过程中高度表达。利用CRISPR/Cas9,我们产生了clps1靶向突变体,该突变体破坏了中期II的染色体分离。这导致二倍体雄性孢子的产生和雄性孢子的异常分裂,最终产生二倍体花粉粒,而雌性减数分裂不受影响。此外,自交受精或将这些突变体作为父本杂交,可以获得三倍体和非整倍体西瓜。我们的研究结果首次证明了2n个配子的分子操纵可以产生三倍体无籽西瓜,为葫芦科和其他物种的多倍体育种和进化研究提供了新的见解。
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来源期刊
Molecular Horticulture
Molecular Horticulture horticultural research-
CiteScore
8.00
自引率
0.00%
发文量
24
审稿时长
12 weeks
期刊介绍: Aims Molecular Horticulture aims to publish research and review articles that significantly advance our knowledge in understanding how the horticultural crops or their parts operate mechanistically. Articles should have profound impacts not only in terms of high citation number or the like, but more importantly on the direction of the horticultural research field. Scope Molecular Horticulture publishes original Research Articles, Letters, and Reviews on novel discoveries on the following, but not limited to, aspects of horticultural plants (including medicinal plants): ▪ Developmental and evolutionary biology ▪ Physiology, biochemistry and cell biology ▪ Plant-microbe and plant-environment interactions ▪ Genetics and epigenetics ▪ Molecular breeding and biotechnology ▪ Secondary metabolism and synthetic biology ▪ Multi-omics dealing with data sets of genome, transcriptome, proteome, metabolome, epigenome and/or microbiome. The journal also welcomes research articles using model plants that reveal mechanisms and/or principles readily applicable to horticultural plants, translational research articles involving application of basic knowledge (including those of model plants) to the horticultural crops, novel Methods and Resources of broad interest. In addition, the journal publishes Editorial, News and View, and Commentary and Perspective on current, significant events and topics in global horticultural fields with international interests.
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