4. (3 pts) represented below is one fragment out of many that has been produced from digesting genomic dna with ecori. inserting this sequence into pgem would involve mixing this fragment with pgem that had also been digested with ecori (question 2) and treating the mixture as before with dna ligase. sketch the circular plasmid that would result from this process. again, be sure to show both strands including the origin of replication, the ampicillin resistance gene and the dna sequences at the restriction sites. mark any restriction sites that will still function.